GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Desulfatiglans anilini DSM 4660

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_028320142.1 H567_RS0102190 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000422285.1:WP_028320142.1
          Length = 354

 Score =  184 bits (467), Expect = 3e-51
 Identities = 128/340 (37%), Positives = 185/340 (54%), Gaps = 22/340 (6%)

Query: 3   YRICLIEGDGIGHEVIPAARRVLEATG----LPLEFVEAEAGWETFERRGTSVPEETVEK 58
           Y I +I GDG G EV+    + LEA G    L  +F   + G E + R GT +P+  + +
Sbjct: 5   YTIGVIPGDGTGPEVVAEGLKALEAAGRKHDLTFDFKRYDLGGEAYLRDGTLLPDSVIHE 64

Query: 59  ILSCHATLFGAATSPTRKVPGFFG--AIRYLRRRLDLYANVRPAK-----SRPVPGSRP- 110
           +    A   GA   P  K PG      +  LR  LDLY N+RP         P+ G +P 
Sbjct: 65  LRGMDAIFLGAIGHPGVK-PGILEREVLLKLRFELDLYINLRPVVLHPGVDTPLMGKQPE 123

Query: 111 GVDLVIVRENTEGLYVE-----QERRYLDVAIADAVISKKASERIGRAALRIAEGRPR-K 164
            +D V+VREN+EG+Y       ++    +VAI ++V ++K  ER  R A   A  R + K
Sbjct: 124 DIDFVVVRENSEGMYAGGGGFFKKGTADEVAIQESVNTRKGVERCIRYAFEYARKRNKGK 183

Query: 165 TLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTN 224
            + +  K NVL     L+    ++VAKDFP +      VD   M ++  PE+FDVIVT N
Sbjct: 184 HVTLCAKTNVLIFESDLWFRVFQDVAKDFPDIGTGYQHVDALCMWMIKNPEQFDVIVTGN 243

Query: 225 LLGDILSDLAAGLVGGLGLAPSGNI-GDTTAVFEPVHGSAPDIAGKGIANPTAAILSAAM 283
           L GDI++D+ A + GGLG+A  GNI    +A+FEP+ GSAP   G+   NP AAI SA M
Sbjct: 244 LFGDIITDIGAIIQGGLGIAAGGNIHPGQSAMFEPIGGSAPKYTGQNKINPMAAIGSAQM 303

Query: 284 MLDYLGEKEAAKRVEKAVDLVLERGPRTPDLG--GDATTE 321
           +L+YLG+ +AA  + +A+  VL +  ++ + G  G  T+E
Sbjct: 304 LLEYLGKDKAAADIFQAIRKVLSQDLKSLEAGRMGYTTSE 343


Lambda     K      H
   0.319    0.137    0.391 

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: 304
Number of extensions: 19
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: 334
Length of database: 354
Length adjustment: 29
Effective length of query: 305
Effective length of database: 325
Effective search space:    99125
Effective search space used:    99125
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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