GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Calditerrivibrio nitroreducens DSM 19672

Align Serine hydroxymethyltransferase; SHMT; Serine methylase; L-threonine/L-allo-threonine aldolase; EC 2.1.2.1; EC 4.1.2.48 (characterized)
to candidate WP_013450717.1 CALNI_RS02960 serine hydroxymethyltransferase

Query= SwissProt::D3DKC4
         (427 letters)



>NCBI__GCF_000183405.1:WP_013450717.1
          Length = 418

 Score =  569 bits (1466), Expect = e-167
 Identities = 275/403 (68%), Positives = 335/403 (83%)

Query: 8   DAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRYYGGCEFV 67
           D EIY+A+ KE ERQ  H+ELIASENF S AV+EAQGS+MTNKYAEG P KRYYGGCEFV
Sbjct: 11  DPEIYDALKKEIERQETHIELIASENFVSPAVLEAQGSIMTNKYAEGYPAKRYYGGCEFV 70

Query: 68  DIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHGGHLTHGA 127
           DIAE+LAI+RAK LF AEHANVQ HSG+QANMAVY AVLKPGDTIMGM+LSHGGHLTHG+
Sbjct: 71  DIAEELAIKRAKELFGAEHANVQAHSGSQANMAVYFAVLKPGDTIMGMNLSHGGHLTHGS 130

Query: 128 KVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDWAKLREIA 187
            VNFSGK++N + YGV+ ET  IDYD+  +LA EHKPKLI+ GASAYPR ID+ K REIA
Sbjct: 131 PVNFSGKLFNVISYGVNKETETIDYDEAEKLATEHKPKLIMVGASAYPRTIDFKKFREIA 190

Query: 188 DSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCKKEFAKDID 247
           D VGA L+VDMAH AGL+A G +P+PVPYA FVT+TTHKTLRGPR G ILCK+E+AK ++
Sbjct: 191 DKVGAVLVVDMAHIAGLVAAGAHPSPVPYADFVTTTTHKTLRGPRGGLILCKEEYAKTLN 250

Query: 248 KSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEGFKVVSGG 307
             +FPGIQGGPLMHVIAAKAVA KEAMS++FK Y  Q+V NA+ L+E  +K GFK+VSGG
Sbjct: 251 SQIFPGIQGGPLMHVIAAKAVALKEAMSEDFKVYQHQIVKNAKRLSERLMKHGFKLVSGG 310

Query: 308 TDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGTPAMTTRG 367
           TD+H++L++L ++ +TG+E EEALG+ANITVNKN VPF+   P  TSG+R+GTPA+TTRG
Sbjct: 311 TDNHLMLINLSNSEITGKEAEEALGRANITVNKNTVPFETRSPFVTSGVRIGTPAVTTRG 370

Query: 368 MKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLY 410
           MKE +M  I  LI++V+ +I  +  I  V+ +V+E+C+QFPLY
Sbjct: 371 MKESEMDFIGDLIAQVLSDIKSDLNINDVKSKVLELCKQFPLY 413


Lambda     K      H
   0.319    0.136    0.395 

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: 622
Number of extensions: 23
Number of successful extensions: 1
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: 427
Length of database: 418
Length adjustment: 32
Effective length of query: 395
Effective length of database: 386
Effective search space:   152470
Effective search space used:   152470
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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