{"id":53321,"date":"2024-03-12T12:05:16","date_gmt":"2024-03-12T12:05:16","guid":{"rendered":"https:\/\/www.almacgroup.com\/api-chemical-development\/?page_id=53321"},"modified":"2025-03-11T15:28:07","modified_gmt":"2025-03-11T15:28:07","slug":"publications","status":"publish","type":"page","link":"https:\/\/www.almacgroup.com\/api-chemical-development\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n<p>Examples of when Almac enzyme engineering technology was used to improve an enzyme<\/p>\n\n\n\n<div style=\"height:32px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-enzyme-engineering-services\">Enzyme Engineering Services<\/h2>\n\n\n<div class=\"o-wrapper\">\n\t<div class=\"o-grid\">\n\n\t\t<div class=\"o-grid__item u-width-full u-align-center\">\n\t\t\t\t\t\t\t<h2 class=\"u-m-b4\">Patents<\/h2>\n\t\t\t\t\t<\/div>\n\n\t<\/div>\n            <div class=\"o-grid u-flex-align-stretch u-m-b3\">\n\n            \n                                            <article class=\"o-grid__item u-width-6\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x4 u-p-y3 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/shc_TOC-1.png\" alt=\"Squalene Hopene Cyclase derivatives and use thereof for producing Ambrox\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 975px; --smush-placeholder-aspect-ratio: 975\/873;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/shc_TOC-1.png\" alt=\"Squalene Hopene Cyclase derivatives and use thereof for producing Ambrox\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Patent<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">Squalene Hopene Cyclase derivatives and use thereof for producing Ambrox<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/squalene-hopene-cyclase-derivatives-and-use-thereof-for-producing-ambrox\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                                            <article class=\"o-grid__item u-width-6\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x4 u-p-y3 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/OLet_MET_TOC-1.png\" alt=\"Cleaning composition comprising an engineered fatty acid alpha-dioxygenase\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 1033px; --smush-placeholder-aspect-ratio: 1033\/902;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/OLet_MET_TOC-1.png\" alt=\"Cleaning composition comprising an engineered fatty acid alpha-dioxygenase\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Patent<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">Cleaning composition comprising an engineered fatty acid alpha-dioxygenase<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/cleaning-composition-comprising-an-engineered-fatty-acid-alpha-dioxygenase-2\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                    <\/div>\n    <\/div>\n\n\n<div class=\"o-wrapper\">\n\t<div class=\"o-grid\">\n\n\t\t<div class=\"o-grid__item u-width-full u-align-center\">\n\t\t\t\t\t\t\t<h2 class=\"u-m-b4\">Technical Publications<\/h2>\n\t\t\t\t\t<\/div>\n\n\t<\/div>\n            <div class=\"o-grid u-flex-align-stretch u-m-b3\">\n\n            \n                                            <article class=\"o-grid__item u-width-3\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x2 u-p-y2 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/CALB_TOC-1.png\" alt=\"Artificial cysteine-lipases with high activity and altered catalytic mechanism created by laboratory evolution\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 754px; --smush-placeholder-aspect-ratio: 754\/883;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/CALB_TOC-1.png\" alt=\"Artificial cysteine-lipases with high activity and altered catalytic mechanism created by laboratory evolution\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Technical Publication<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">Artificial cysteine-lipases with high activity and altered catalytic mechanism created by laboratory evolution<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/artificial-cysteine-lipases-with-high-activity-and-altered-catalytic-mechanism-created-by-laboratory-evolution\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                                            <article class=\"o-grid__item u-width-3\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x2 u-p-y2 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/P253F_G254A_R258M_L443F_2phenylhexanone_rep0_final_TOC_-1.png\" alt=\"Spatial requirement for PAMO for transformation of non-native linear substrate\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 1365px; --smush-placeholder-aspect-ratio: 1365\/1000;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/P253F_G254A_R258M_L443F_2phenylhexanone_rep0_final_TOC_-1.png\" alt=\"Spatial requirement for PAMO for transformation of non-native linear substrate\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Technical Publication<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">Spatial requirement for PAMO for transformation of non-native linear substrate<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/spatial-requirement-for-pamo-for-transformation-of-non-native-linear-substrate\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                                            <article class=\"o-grid__item u-width-3\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x2 u-p-y2 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/TOC_Nitrilase_web.png\" alt=\"Enzyme Optimization and Process Development for a Scalable Synthesis of (R)\u20112-Methoxymandelic Acid\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 1080px; --smush-placeholder-aspect-ratio: 1080\/1080;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/TOC_Nitrilase_web.png\" alt=\"Enzyme Optimization and Process Development for a Scalable Synthesis of (R)\u20112-Methoxymandelic Acid\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Technical Publication<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">Enzyme Optimization and Process Development for a Scalable Synthesis of (R)\u20112-Methoxymandelic Acid<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/enzyme-optimization-and-process-development-for-a-scalable-synthesis-of-r%e2%80%912-methoxymandelic-acid\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                                            <article class=\"o-grid__item u-width-3\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x2 u-p-y2 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/TOC_TAM_Square_1.png\" alt=\"Rational Design of a (S)-Selective-Transaminase for Asymmetric Synthesis of (1S)-1-(1,1\u2032-biphenyl-2-yl)ethanamine\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 1080px; --smush-placeholder-aspect-ratio: 1080\/1080;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/TOC_TAM_Square_1.png\" alt=\"Rational Design of a (S)-Selective-Transaminase for Asymmetric Synthesis of (1S)-1-(1,1\u2032-biphenyl-2-yl)ethanamine\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Technical Publication<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">Rational Design of a (S)-Selective-Transaminase for Asymmetric Synthesis of (1S)-1-(1,1\u2032-biphenyl-2-yl)ethanamine<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/rational-design-of-a-s-selective-transaminase-for-asymmetric-synthesis-of-1s-1-11%e2%80%b2-biphenyl-2-ylethanamine\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                                            <article class=\"o-grid__item u-width-3\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x2 u-p-y2 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/MSR_case_study-1.png\" alt=\"Rational Mutagenesis of Methionine Sulfoxide Reductase\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 515px; --smush-placeholder-aspect-ratio: 515\/472;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/MSR_case_study-1.png\" alt=\"Rational Mutagenesis of Methionine Sulfoxide Reductase\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Technical Publication<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">Rational Mutagenesis of Methionine Sulfoxide Reductase<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/discovery-and-rational-mutagenesis-of-methionine-sulfoxide-reductase-biocatalysts-to-expand-the-substrate-scope-of-the-kinetic-resolution-of-chiral-sulfoxides\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                                            <article class=\"o-grid__item u-width-3\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x2 u-p-y2 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/carboxylesterase_TOC-1.png\" alt=\"Rational engineering of a carboxylesterase for the synthesis of polyesters for biomedical applications\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 840px; --smush-placeholder-aspect-ratio: 840\/849;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/carboxylesterase_TOC-1.png\" alt=\"Rational engineering of a carboxylesterase for the synthesis of polyesters for biomedical applications\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Technical Publication<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">Rational engineering of a carboxylesterase for the synthesis of polyesters for biomedical applications<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/rational-engineering-of-a-carboxylesterase-for-the-synthesis-of-polyesters-for-biomedical-applications\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                                            <article class=\"o-grid__item u-width-3\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x2 u-p-y2 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/oligo_TOC-2-1.png\" alt=\"Towards the enzymatic synthesis of oligonucleotides | Manufacturing Chemist\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 268px; --smush-placeholder-aspect-ratio: 268\/250;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/oligo_TOC-2-1.png\" alt=\"Towards the enzymatic synthesis of oligonucleotides | Manufacturing Chemist\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Technical Publication<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">Towards the enzymatic synthesis of oligonucleotides | Manufacturing Chemist<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/towards-the-enzymatic-synthesis-of-oligonucleotides-manufacturing-chemist\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                                            <article class=\"o-grid__item u-width-3\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x2 u-p-y2 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/P450_BM3_TOC-1.png\" alt=\"Regio- and stereoselectivity in the CYP450BM3-catalyzed hydroxylation of complex terpenoids: a QM\/MM study\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 965px; --smush-placeholder-aspect-ratio: 965\/829;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/P450_BM3_TOC-1.png\" alt=\"Regio- and stereoselectivity in the CYP450BM3-catalyzed hydroxylation of complex terpenoids: a QM\/MM study\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Technical Publication<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">Regio- and stereoselectivity in the CYP450BM3-catalyzed hydroxylation of complex terpenoids: a QM\/MM study<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/regio-and-stereoselectivity-in-the-cyp450bm3-catalyzed-hydroxylation-of-complex-terpenoids-a-qm-mm-study\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                                            <article class=\"o-grid__item u-width-3\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x2 u-p-y2 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/TOC_PAMO-1.png\" alt=\"Catalytic mechanism of phenylacetone monooxygenases for non-native linear substrates\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 268px; --smush-placeholder-aspect-ratio: 268\/250;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2024\/03\/TOC_PAMO-1.png\" alt=\"Catalytic mechanism of phenylacetone monooxygenases for non-native linear substrates\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Technical Publication<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">Catalytic mechanism of phenylacetone monooxygenases for non-native linear substrates<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/catalytic-mechanism-of-phenylacetone-monooxygenases-for-non-native-linear-substrates\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                                            <article class=\"o-grid__item u-width-3\/12 u-width-4\/12@l u-width-6\/12@m u-width-full@s u-flex u-m-b3 u-a-full\">\n                    <div class=\"c-related-resources__panel u-flex u-flex-direction-column u-flex-align-center u-align-center u-p-x2 u-p-y2 u-m-b2\">\n                \n                                                <img decoding=\"async\" class=\"u-m-b2 lazyload\" data-src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2025\/01\/biostructnet_square_tile.jpg\" alt=\"BioStructNet: Structure-Based Network with Transfer Learning for Predicting Biocatalyst Functions\" src=\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\" style=\"--smush-placeholder-width: 839px; --smush-placeholder-aspect-ratio: 839\/839;\"><noscript><img decoding=\"async\" class=\"u-m-b2\" src=\"https:\/\/www.almacgroup.com\/api-chemical-development\/wp-content\/uploads\/sites\/4\/2025\/01\/biostructnet_square_tile.jpg\" alt=\"BioStructNet: Structure-Based Network with Transfer Learning for Predicting Biocatalyst Functions\"><\/noscript>\n                        \n                                                    <p class=\"c-resource__category\">Technical Publication<\/p>\n                        \n                                                    <h4 class=\"u-m-t2\">BioStructNet: Structure-Based Network with Transfer Learning for Predicting Biocatalyst Functions<\/h4>\n                        \n                        \n                                                                                                                        <a class=\"u-m-t-auto c-btn c-btn-primary c-btn--red\" href=\"https:\/\/www.almacgroup.com\/knowledge\/library\/biostructnet-structure-based-network-with-transfer-learning-for-predicting-biocatalyst-functions\/\" target=\"\">Read now<\/a>\n                                                                                                        <\/div> <!-- \/c-related-resoucres__panel -->\n                    <\/article>\n                    <\/div>\n    <\/div>\n\n\n\n<style>.c-related-resources__panel img {\n    height: 250px !important;\n    width: 268px !important;\n    object-fit: cover;\n}\n<\/style>\n\n\n\t<div class=\"\">\n\t\t<div class=\"o-wrapper\">\n\t\t\t<div class=\"o-grid\">\n\t\t\t\t<div class=\"o-grid__item u-width-full\">\n\t\t\t\t\t<div class=\"s-cms\">\n\t\t\t\t\t\t\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t<\/div>\n\n\t\n","protected":false},"excerpt":{"rendered":"<p>Examples of when Almac enzyme engineering technology was used to improve an enzyme Enzyme Engineering Services<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-53321","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v25.3.1 (Yoast SEO v26.3) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Publications - API Services &amp; 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