GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Hydrogenophaga taeniospiralis NBRC 102512

Align Putrescine aminotransferase; PAT; PATase; EC 2.6.1.82; Cadaverine transaminase; EC 2.6.1.-; Putrescine transaminase; Putrescine--2-oxoglutaric acid transaminase (uncharacterized)
to candidate WP_084236011.1 HTA01S_RS10480 4-aminobutyrate--2-oxoglutarate transaminase

Query= curated2:B7LZM2
         (459 letters)



>NCBI__GCF_001592305.1:WP_084236011.1
          Length = 431

 Score =  196 bits (498), Expect = 1e-54
 Identities = 131/339 (38%), Positives = 189/339 (55%), Gaps = 31/339 (9%)

Query: 76  LVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLR--AMLAKTV 133
           L D +G+ FID  GG  + N GH +P V +A+  QL +   HS   + P      LA+ +
Sbjct: 44  LWDIEGRRFIDFAGGIAVLNTGHVHPKVQAAIAAQLQRFT-HSCYQVVPYAEYVSLAERI 102

Query: 134 AALTP--GKLKYSFFCNSGTESVEAALKLAKAYQSPRGKFTFIATSGAFHGKSLGALSAT 191
            A+ P  GK K +FF ++G E++E A+K+A+   S  G+   IA  GAFHG+SL A+S T
Sbjct: 103 NAIVPIEGKAKTAFF-STGAEAIENAIKIAR---SSTGRSGVIAFGGAFHGRSLFAVSLT 158

Query: 192 AK-STFRKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDV----------AAVILEPI 240
            K   ++  F P  P   HVPF    A   +L+E K+  D V          AA++ EP+
Sbjct: 159 GKVQPYKAGFGPFPPEIYHVPF---PAEGASLDETKRAMDHVFKCDIEPSRVAAIVFEPV 215

Query: 241 QGEGGVILPPPGYLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAK 300
           QGEGG        +  +R LCD+ G L+I DEVQTG  RTG+MFA EH  V PD++ +AK
Sbjct: 216 QGEGGFNPIQKDAVLWLRALCDQHGILLIADEVQTGFARTGRMFAMEHYGVSPDLMTMAK 275

Query: 301 ALGGGVMPIGATIATEEVFSVLFDNPFLHTT--TFGGNPLACAAALATINVLLEQNLPAQ 358
           ++ G     G T++     + + D P       T+ GNPLA AA+ A ++V+ E+ LP +
Sbjct: 276 SMAG-----GTTLSAVSGKAAIMDGPAPGGLGGTYAGNPLAIAASHAVLDVMAEEKLPER 330

Query: 359 AEQKGDMLLDGFRQLAREYPDLVQEARGKGMLMAIEFVD 397
           A++ GD L+   R    +YP  + E RG G ++A EFVD
Sbjct: 331 AQRLGDQLVAHLRAAKAKYP-RIGEVRGLGAMVACEFVD 368


Lambda     K      H
   0.320    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: 469
Number of extensions: 23
Number of successful extensions: 7
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: 459
Length of database: 431
Length adjustment: 32
Effective length of query: 427
Effective length of database: 399
Effective search space:   170373
Effective search space used:   170373
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: 51 (24.3 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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