GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Sedimenticola selenatireducens DSM 17993

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_029132623.1 A3GO_RS0105910 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000428045.1:WP_029132623.1
          Length = 360

 Score =  211 bits (538), Expect = 2e-59
 Identities = 144/365 (39%), Positives = 204/365 (55%), Gaps = 38/365 (10%)

Query: 1   MAYRICLIEGDGIGHEVIPAARRVLEAT----GLPLEFVEAEAGWETFERRGTSVPEETV 56
           M+  I ++ GDGIG E++  A +VL       GL +E  EA  G   ++  G  +PE T+
Sbjct: 1   MSKNILVLPGDGIGQEIVTEAVKVLACLRDDYGLDIEMDEALIGGTAYDAAGHPLPEATL 60

Query: 57  EKILSCHATLFGAATSP--------TRKVPGFFGAIRYLRRRLDLYANVRPAKSRPV--- 105
                  A L GA   P         R   G  G    +R+ L L+AN+RPA   P    
Sbjct: 61  NLAREADAVLLGAVGGPKWEPLDISVRPEKGLLG----IRKELGLFANLRPAILYPQLAD 116

Query: 106 -----PGSRPGVDLVIVRENTEGLYVEQER--RYLDVAIADA----VISKKASERIGRAA 154
                P    G+D++IVRE T G+Y  Q R  R L+    +     +  +   +RI R A
Sbjct: 117 ASTLRPEVVSGLDIMIVRELTGGIYFGQPRGVRVLENGEKEGFNTLIYKESEVDRIVRVA 176

Query: 155 LRIAEGRPRKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRP 214
           + IA  R ++   +  KANVL  T+ ++ +   +V  D+P V +  + VDN AMQLV  P
Sbjct: 177 MDIAMKRNKRVCSV-DKANVLECTE-MWREVAVKVGADYPEVELSHMYVDNAAMQLVRAP 234

Query: 215 ERFDVIVTTNLLGDILSDLAAGLVGGLGLAPSGNIGDT-TAVFEPVHGSAPDIAGKGIAN 273
           ++FDV+VTTN+ GDILSD A+ L G +G+ PS ++ +    ++EP+HGSAPDIAG+G+AN
Sbjct: 235 KQFDVMVTTNMFGDILSDCASMLTGSIGMLPSASLDENGKGMYEPIHGSAPDIAGQGVAN 294

Query: 274 PTAAILSAAMMLDY-LGEKEAAKRVEKAVDLVLERGPRTPDLGGDAT----TEAFTEAVV 328
           P A ILS AMML Y L E   A RVE+AV+  L++G RTPD+  + T    TEA  +AVV
Sbjct: 295 PLATILSVAMMLRYSLDEDAMADRVEQAVNKTLDQGLRTPDIYSEGTRKVGTEAMGDAVV 354

Query: 329 EALKS 333
            AL++
Sbjct: 355 AALRA 359


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: 302
Number of extensions: 13
Number of successful extensions: 6
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: 360
Length adjustment: 29
Effective length of query: 305
Effective length of database: 331
Effective search space:   100955
Effective search space used:   100955
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 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