GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Rhodomicrobium vannielii ATCC 17100

Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_013419981.1 RVAN_RS11970 aspartate aminotransferase family protein

Query= reanno::WCS417:GFF4238
         (406 letters)



>NCBI__GCF_000166055.1:WP_013419981.1
          Length = 393

 Score =  339 bits (869), Expect = 1e-97
 Identities = 176/375 (46%), Positives = 240/375 (64%), Gaps = 5/375 (1%)

Query: 30  RGEGSRVWDQAGRELIDFAGGIAVNVLGHAHPALVGALTEQAHKLWHVSNVFTNEPALRL 89
           RGEG+ +   AG   +DF  G+AVN LGHAHP L+ ALTEQAHK+WH SN++      RL
Sbjct: 17  RGEGAWLETAAGERYLDFGSGVAVNALGHAHPHLIAALTEQAHKVWHTSNLYRVPGQERL 76

Query: 90  AHKLIDATFAERVFFCNSGAEANEAAFKLARRVAFDRFGSEKYEIIAALNSFHGRTLFTV 149
           A +L   TFA++VFF NSGAEA E + K+AR+        E++ +I  +++FHGRTL T+
Sbjct: 77  AERLCALTFADKVFFTNSGAEAMECSIKMARKYHSYNGQPERWRVITFVDAFHGRTLATI 136

Query: 150 NVGGQSKYSDGFGPKITGITHVPYNDLDALKAAVSDKTCAVVLEPIQGEGGVLPAELAYL 209
             G Q K+  GFGPK+ G   VP  DLDAL+AA++ +T A+++EPIQGE GV P    +L
Sbjct: 137 AAGNQEKHLKGFGPKVDGFDQVPVGDLDALRAAITHETAALLIEPIQGESGVRPVGWPFL 196

Query: 210 QGARDLCDANNALLVFDEVQTGMGRSGHLFAYQHYGVTPDILTSAKSLGGGFPIAAMLTT 269
           +  R++ D +  LL+ DEVQTG+GR+G LFA++  G+ PDI+  AK +GGGFP+ A L T
Sbjct: 197 RALREIADEHGLLLILDEVQTGVGRTGKLFAHEWAGIEPDIMGIAKGIGGGFPVGACLAT 256

Query: 270 EALAKHLVVGTHGTTYGGNPLACAVAEAVIDVINTPEVLAGVNAKHDLFKARL-EQIGKQ 328
           E  A  +  G+HG+T+GGNPLA AVA AV+D+   PE L  V     LFK RL E I + 
Sbjct: 257 EKAASGMTAGSHGSTFGGNPLAMAVANAVLDIATKPEFLGNVQEMSLLFKQRLAEIIDRH 316

Query: 329 YGIFTEVRGMGLLLGCVLSDAFKGKAKDVFNAAEKENLMILQAGPDVVRFAPSLVVEDAD 388
             I  ++RG GLLLG       K  + DV +    E L+ + AG +VVR  P L+V +A+
Sbjct: 317 PRIIADIRGEGLLLGL----KCKVPSADVSSTLFAEKLLTVSAGDNVVRLLPPLIVTEAE 372

Query: 389 IKEGLDRFERAVKAL 403
           IK+  ++ E A   L
Sbjct: 373 IKDACEKIESACARL 387


Lambda     K      H
   0.320    0.137    0.400 

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: 429
Number of extensions: 21
Number of successful extensions: 3
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: 406
Length of database: 393
Length adjustment: 31
Effective length of query: 375
Effective length of database: 362
Effective search space:   135750
Effective search space used:   135750
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