GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rocD in Erythrobacter gangjinensis K7-2

Align Ornithine aminotransferase; OAT; EC 2.6.1.13; Ornithine--oxo-acid aminotransferase (uncharacterized)
to candidate WP_047007017.1 AAW01_RS09055 aspartate aminotransferase family protein

Query= curated2:C3P3K3
         (396 letters)



>NCBI__GCF_001010925.1:WP_047007017.1
          Length = 396

 Score =  234 bits (597), Expect = 3e-66
 Identities = 137/362 (37%), Positives = 202/362 (55%), Gaps = 7/362 (1%)

Query: 36  DPEGNRYMDLLSAYSAVNQGHRHPKIINALIDQANRVTLTSRAFHSDQLGPWYEKVAKLT 95
           D  G RY+D  S  +    GH H  +I+A+ DQA+R+   S  + S Q     +K+   T
Sbjct: 27  DENGTRYLDFASGIAVNLLGHSHKGLISAIQDQASRLMHVSNLYGSPQGEALAQKLVDHT 86

Query: 96  NKEMVLPMNTGAEAVETAIKTARRWAYDVKKVEANRAEIIVCEDNFHGRTMGAVSMSSNE 155
             + V   N+GAE+VE AIKTAR  AY   +    R EII  ++ FHGRTM  +S S+ E
Sbjct: 87  FADTVFFTNSGAESVECAIKTAR--AYHQHEGNEERFEIITFKNAFHGRTMATISASNQE 144

Query: 156 EYKRGFGPMLPGIIVIPYGDLEALKAAITPNTAAFILEPIQGEAGINIPPAGFLKEALEV 215
           +  +GF P+LPG   + + DLE  KAAI P+TA F++EPIQGE GI     GF+K   E+
Sbjct: 145 KMHKGFNPLLPGFTYVEFDDLEGAKAAIGPHTAGFLVEPIQGEGGIRPASEGFMKGLREL 204

Query: 216 CKKENVLFVADEIQTGLGRTGKVFACDWDNVTPDMYILGKALGGGVFPISCAAANRDILG 275
             + +++   DE+Q G+ RTGK+FA +   + PD+    K LGGG FP+    A      
Sbjct: 205 ADEHDLMLALDEVQCGVARTGKLFAYENYGIEPDILASAKGLGGG-FPMGACLATEKAAR 263

Query: 276 VFEPGSHGSTFGGNPLACAVSIAALEVLEEEKLTERSLQLGEKLVGQLKE-IDN--PMIT 332
               G+HGST+GGNPLA A   A ++ +   +  E     GE+L  ++++ I N   +  
Sbjct: 264 GMVFGTHGSTYGGNPLAMAAGNAVMDAVANPEFLEEVRAKGERLRSRIEQFIGNYPDLFE 323

Query: 333 EVRGKGLFIGIELNEPARPYCEQLK-AAGLLCKETHENVIRIAPPLVISEEDLEWAFQKI 391
            VRG GL +GI +    RP+   L+    LL     ++ +R+ PPLVI + +++  F+K+
Sbjct: 324 SVRGMGLMLGIRMKVEPRPFMVHLRDNHELLMVAAGDHTLRVLPPLVIGDAEMDEFFEKL 383

Query: 392 KA 393
            A
Sbjct: 384 SA 385


Lambda     K      H
   0.317    0.136    0.402 

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: 386
Number of extensions: 22
Number of successful extensions: 5
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: 396
Length of database: 396
Length adjustment: 31
Effective length of query: 365
Effective length of database: 365
Effective search space:   133225
Effective search space used:   133225
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 50 (23.9 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