GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Methylomonas methanica MC09

Align branched-chain-amino-acid aminotransferase; EC 2.6.1.42 (characterized)
to candidate WP_041364244.1 METME_RS12940 branched-chain amino acid transaminase

Query= CharProtDB::CH_024500
         (309 letters)



>NCBI__GCF_000214665.1:WP_041364244.1
          Length = 308

 Score =  273 bits (699), Expect = 3e-78
 Identities = 136/301 (45%), Positives = 194/301 (64%), Gaps = 2/301 (0%)

Query: 8   YIWFNGEMVRWEDAKVHVMSHALHYGTSVFEGIRCYDSHKGPVVFRHREHMQRLHDSAKI 67
           +IW +G+ V W +AKVHV++H LHYG  VFEG+R Y +  G  +F+  EH  RL+ SA I
Sbjct: 10  WIWLDGQWVEWREAKVHVLTHTLHYGCGVFEGLRAYKTDNGTAIFKLPEHTDRLYRSAHI 69

Query: 68  YRFPVSQSIDELMEACRDVIRKNNLTSAYIRPLIFVGDVGMGVNPPAGYSTDVIIAAFPW 127
               +  S +EL +A +D + KNNL SAYIR ++F G  GMG+         V++AA+ W
Sbjct: 70  MNMKMPFSKEELNQAHKDAVAKNNLDSAYIRSMVFFGSEGMGLRAD-NLKVHVMVAAWTW 128

Query: 128 GAYLGAEALEQGIDAMVSSWNRAAPNTIPTAAKAGGNYLSSLLVGSEARRHGYQEGIALD 187
           GAYLGAE +E+GI    SS+ R   N+    AKA GNY++S+L   EA   GY E + LD
Sbjct: 129 GAYLGAENMEKGIRIRTSSYTRNHVNSTMCKAKANGNYINSILALQEALSTGYDEALLLD 188

Query: 188 VNGYISEGAGENLFEVKDGVLFTPPFTSSALPGITRDAIIKLAKELGIEVREQVLSRESL 247
             G+ +EG+GENLF V++G ++TP  T+SAL GITRD +I +A+E G EV E+ ++R+ +
Sbjct: 189 HEGFCAEGSGENLFIVRNGKIYTPE-TTSALEGITRDTLITIAREQGYEVIEKRITRDEV 247

Query: 248 YLADEVFMSGTAAEITPVRSVDGIQVGEGRCGPVTKRIQQAFFGLFTGETEDKWGWLDQV 307
           Y+ADE F +G+AAE+TP+R  D   +G G  GP+T+++Q  +F    G   D   WL  V
Sbjct: 248 YVADEAFFTGSAAEVTPIRQYDNRDIGSGSRGPITEKLQTLYFDYVHGRRADHKDWLSLV 307

Query: 308 N 308
           +
Sbjct: 308 S 308


Lambda     K      H
   0.319    0.136    0.413 

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: 305
Number of extensions: 12
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: 309
Length of database: 308
Length adjustment: 27
Effective length of query: 282
Effective length of database: 281
Effective search space:    79242
Effective search space used:    79242
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: 48 (23.1 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 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