GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metC in Sulfurihydrogenibium azorense Az-Fu1

Align glutamine-pyruvate transaminase (EC 2.6.1.15); kynurenine-oxoglutarate transaminase (EC 2.6.1.7); cysteine-S-conjugate beta-lyase (EC 4.4.1.13) (characterized)
to candidate WP_012674279.1 SULAZ_RS01475 pyridoxal phosphate-dependent aminotransferase

Query= BRENDA::Q71RI9
         (455 letters)



>NCBI__GCF_000021545.1:WP_012674279.1
          Length = 391

 Score =  157 bits (396), Expect = 8e-43
 Identities = 110/353 (31%), Positives = 172/353 (48%), Gaps = 27/353 (7%)

Query: 66  VVNLGQGFPDISPPSYVKEELSKAAFIDNMNQYTRGFGHPALVKALSCLYGKIYQRQIDP 125
           +++ G G PD   P +VKE   KA   +   +YT   G P L +A++            P
Sbjct: 32  IISFGAGEPDFDTPDFVKEAAIKA-LKEGKTKYTAAAGIPQLREAIAQKLKTRNNIDYSP 90

Query: 126 NEEILVAVGAYGSLFNSIQGLVDPGDEVIIMVPFYDCYEPMVRMAGAVPVFIPLRSKPTD 185
           +E ++V  GA   L+     L++PGDEVI+  P++  Y   + +     V   L  +  +
Sbjct: 91  SE-VIVVPGAKMGLYEIFAILLNPGDEVIVPAPYWVSYTEQIALNDGESVIPQLSEE--N 147

Query: 186 GMKWTSSDWTFDPRELESKFSSKTKAIILNTPHNPLGKVYTRQELQVIADLCVKHDTLCI 245
           G   T+         +ES  + KTKA++LNTP NP G V  ++EL+ IA++C+KH  + I
Sbjct: 148 GFVLTADI-------VESSITPKTKALVLNTPSNPTGAVIPKKELEKIAEVCLKHSIMII 200

Query: 246 SDEVYEWLVYTGHTHVKIATL-PGMWERTITIGSAGKTFSVTGWKLGWSIGPAHLIKHLQ 304
           SDE YE   Y G  HV IA+L   + E T T+G+  K++S+TGW+LGW   P   IK + 
Sbjct: 201 SDECYEEFSY-GEPHVSIASLSKEVREITFTVGAFSKSYSMTGWRLGWVAAPEKYIKAMT 259

Query: 305 TVQQNSFYTCATPLQAALAEAFWIDIKRMDDPECYFNSLPKELEVKRDRMVRLLNSV-GL 363
            +Q  +     T  Q    EA       + D   +   +  E   +RD +V  LNS+ G+
Sbjct: 260 NIQSQTISNPTTFAQYGALEA-------LKDNGQFPAMMRSEFMKRRDYIVEALNSIKGI 312

Query: 364 KPIVPDGGYFIIADVSSLGADLSDMNSDEPYDYKFVKWMTKHKKLTAIPVSAF 416
           K   P+G ++   +VS        +  D   D     ++ +  K+  +P SAF
Sbjct: 313 KCTKPEGAFYAFPNVSYY------IKGDIKNDIDLTTYLLEEGKVAVVPGSAF 359


Lambda     K      H
   0.320    0.136    0.419 

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: 402
Number of extensions: 29
Number of successful extensions: 4
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: 455
Length of database: 391
Length adjustment: 32
Effective length of query: 423
Effective length of database: 359
Effective search space:   151857
Effective search space used:   151857
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