GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpB in Derxia gummosa DSM 723

Align isocitrate lyase (EC 4.1.3.1) (characterized)
to candidate WP_028311044.1 H566_RS0108095 isocitrate lyase

Query= BRENDA::P9WKK7
         (428 letters)



>NCBI__GCF_000482785.1:WP_028311044.1
          Length = 430

 Score =  587 bits (1514), Expect = e-172
 Identities = 288/421 (68%), Positives = 345/421 (81%), Gaps = 2/421 (0%)

Query: 8   KSAEQIQQEWDTNPRWKDVTRTYSAEDVVALQGSVVEEHTLARRGAEVLWEQLHDLEWVN 67
           + A+Q+Q++W+ NPRWK + R YSAEDVV L+GS+  EHTLA+RGAE LW  +    +VN
Sbjct: 6   EQAQQLQKDWNENPRWKGIQRGYSAEDVVRLRGSIQIEHTLAKRGAEKLWNLITTEPFVN 65

Query: 68  ALGALTGNMAVQQVRAGLKAIYLSGWQVAGDANLSGHTYPDQSLYPANSVPQVVRRINNA 127
           ALGALTGN A+QQV+AGLKAIYLSGWQVAGDANL+G  YPDQSLYPANSVP VVRRINN 
Sbjct: 66  ALGALTGNQAMQQVKAGLKAIYLSGWQVAGDANLAGEMYPDQSLYPANSVPAVVRRINNT 125

Query: 128 LQRADQIAKIEGDTSVENWLAPIVADGEAGFGGALNVYELQKALIAAGVAGSHWEDQLAS 187
            QRADQI   EG    + + APIVAD EAGFGG LN +EL K++I AG AG H+EDQLAS
Sbjct: 126 FQRADQIQWSEGKGDTD-FFAPIVADAEAGFGGVLNAFELMKSMIEAGAAGVHFEDQLAS 184

Query: 188 EKKCGHLGGKVLIPTQQHIRTLTSARLAADVADVPTVVIARTDAEAATLITSDVDERDQP 247
            KKCGH+GGKVL+PT+  +  L +ARLAADV  VPTV++ARTDAEAA LIT+DVD+ D+P
Sbjct: 185 VKKCGHMGGKVLVPTRDAVAKLVAARLAADVMGVPTVLVARTDAEAADLITTDVDDNDKP 244

Query: 248 FITGERTREGFYRTKNGIEPCIARAKAYAPFADLIWMETGTPDLEAARQFSEAVKAEYPD 307
           F+TGERT EGF+RTK G+E  I+R  AYAP+ADLIW ETG PDLE A+ F+EA+  ++P 
Sbjct: 245 FLTGERTVEGFFRTKPGLEQAISRGLAYAPYADLIWCETGKPDLEYAKNFAEAIHKKFPG 304

Query: 308 QMLAYNCSPSFNWKKHLDDATIAKFQKELAAMGFKFQFITLAGFHALNYSMFDLAYGYAQ 367
           +ML+YNCSPSFNWKK+LDDATIAKFQKEL AMG+KFQFITLAGFHALNYSMF+LA+GYA+
Sbjct: 305 KMLSYNCSPSFNWKKNLDDATIAKFQKELGAMGYKFQFITLAGFHALNYSMFNLAHGYAR 364

Query: 368 NQMSAYVELQEREFAAEERGYTATKHQREVGAGYFDRIATTVD-PNSSTTALTGSTEEGQ 426
            QM A+VELQ+ EFAA ++G+TA KHQREVG GYFD +   ++   SSTTAL GSTE+ Q
Sbjct: 365 EQMKAFVELQQAEFAAADKGFTAVKHQREVGTGYFDAVTQCIEGGQSSTTALKGSTEDEQ 424

Query: 427 F 427
           F
Sbjct: 425 F 425


Lambda     K      H
   0.316    0.130    0.384 

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: 655
Number of extensions: 24
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: 428
Length of database: 430
Length adjustment: 32
Effective length of query: 396
Effective length of database: 398
Effective search space:   157608
Effective search space used:   157608
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: 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