Align glycine hydroxymethyltransferase (EC 2.1.2.1) (characterized)
to candidate WP_044414093.1 NA59_RS13695 serine hydroxymethyltransferase
Query= BRENDA::L7Y8B0 (417 letters) >NCBI__GCF_000934765.1:WP_044414093.1 Length = 423 Score = 627 bits (1617), Expect = 0.0 Identities = 315/423 (74%), Positives = 350/423 (82%), Gaps = 6/423 (1%) Query: 1 MFSKQDQIQGYDDALLAAMNAEEQRQEDHIELIASENYTSKRVMQAQGSGLTNKYAEGYP 60 MF K I GYDD + AM AE QRQEDHIELIASENYTS RVM AQGS LTNKYAEGYP Sbjct: 1 MFDKTMTIAGYDDDIANAMAAEAQRQEDHIELIASENYTSPRVMAAQGSVLTNKYAEGYP 60 Query: 61 GKRYYGGCEHVDKVEALAIERAKQLFGADYANVQPHSGSSANGAVYLALVQAGDTILGMS 120 KRYYGGCEHVD VEALAIERAKQLFGADYANVQPHSGS AN V++AL++ GDT+LGMS Sbjct: 61 YKRYYGGCEHVDVVEALAIERAKQLFGADYANVQPHSGSQANAPVFMALLEPGDTVLGMS 120 Query: 121 LAHGGHLTHGAKVSSSGKLYNAVQYGIDTNTGLIDYDEVERLAVEHKPKMIVAGFSAYSK 180 LAHGGHLTHG+KV+ SGK+YNAVQYG+ TG IDY+EV+RLA EHKPK+++AGFSAYS+ Sbjct: 121 LAHGGHLTHGSKVNFSGKIYNAVQYGLKPETGEIDYNEVQRLATEHKPKLVIAGFSAYSQ 180 Query: 181 TLDFPRFRAIADKVGALLFVDMAHVAGLVAAGLYPNPIPFADVVTTTTHKTLRGPRGGLI 240 +D+ RFR IAD VGA L VDMAHVAGLVAAGLYPNP+ ADV TTTTHKTLRGPRGGLI Sbjct: 181 IVDWQRFRDIADSVGAYLLVDMAHVAGLVAAGLYPNPVQIADVTTTTTHKTLRGPRGGLI 240 Query: 241 LAKANEEIEKKLNAAVFPGAQGGPLMHVIAAKAVCFKEALEPEFKAYQQQVIENAQAMAQ 300 LAKAN EIEKKLN+ VFPG QGGPLMHVIAAKAV FKEA+EPEFK Y QVI+NAQAMAQ Sbjct: 241 LAKANPEIEKKLNSLVFPGTQGGPLMHVIAAKAVAFKEAMEPEFKTYAAQVIKNAQAMAQ 300 Query: 301 VFVDRGYDVVSGGTDNHLFLVSLIRQGLTGKDADAALGCAHITVNKNAVPNDPQSPFVTS 360 VF++RG DVVSGGT NHLFLVSLI +GLTGK DAALG AHIT+NKN+VPNDP SPFVTS Sbjct: 301 VFIERGLDVVSGGTQNHLFLVSLIEKGLTGKLVDAALGAAHITINKNSVPNDPMSPFVTS 360 Query: 361 GLRIGTPAVTTRGFKVAQCVALAGWICDILDNLGDAD------VEADVAKNVAALCADFP 414 G+RIGT A TTRGF +C LAGW+CD+++ A V A V V+ALCA P Sbjct: 361 GIRIGTAAATTRGFGEQECRDLAGWMCDVVNACDQASESWDEAVIAQVRDKVSALCAAHP 420 Query: 415 VYR 417 VY+ Sbjct: 421 VYK 423 Lambda K H 0.318 0.134 0.390 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 623 Number of extensions: 21 Number of successful extensions: 2 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 417 Length of database: 423 Length adjustment: 32 Effective length of query: 385 Effective length of database: 391 Effective search space: 150535 Effective search space used: 150535 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory