GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Cupriavidus basilensis 4G11

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate RR42_RS33755 RR42_RS33755 tartrate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>FitnessBrowser__Cup4G11:RR42_RS33755
          Length = 358

 Score =  216 bits (549), Expect = 9e-61
 Identities = 141/351 (40%), Positives = 194/351 (55%), Gaps = 26/351 (7%)

Query: 3   YRICLIEGDGIGHEVIPAARRVLEAT-----GLPLEFVEAEAGWETFERRGTSVPEETVE 57
           Y+I  I GDGIG EVI A  +VLE       G  L         + +  +G  +PE  +E
Sbjct: 4   YKIAAIPGDGIGPEVISAGLQVLETLAGQDGGFKLGVEHFPWSSDYYLEKGYYIPEGGLE 63

Query: 58  KILSCHATLFGAATSPTRKVP---GFFGAIRYLRRRLDLYANVRPAKSRPVPGSRP---- 110
           ++    A  FGA  +    VP     +G    + +  D YANVRPA  R +PG +     
Sbjct: 64  RLKQFDAIFFGAVGA--LNVPDHVSLWGLRLPIAQGFDQYANVRPA--RVLPGVKSPLAN 119

Query: 111 --GVDLVIVRENTEGLYVEQERRY-----LDVAIADAVISKKASERIGRAALRIAEGRPR 163
              +D VI+REN+EG Y     R      ++     AV ++   ERI R A  IA+ RPR
Sbjct: 120 GKDIDWVIIRENSEGEYAGNGGRTHRGLPIETGTETAVFTRAGVERIHRFAFEIAQKRPR 179

Query: 164 KTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTT 223
           K L +  K+N       ++ +   EVAKD+P V V   +VD    ++V++P   DV+V T
Sbjct: 180 KHLTLVTKSNAQRFGMVMWDEIFYEVAKDYPDVKVDRELVDAVTTRMVLKPHTLDVVVAT 239

Query: 224 NLLGDILSDLAAGLVGGLGLAPSGNIGDTT---AVFEPVHGSAPDIAGKGIANPTAAILS 280
           NL  DILSDLAA L G LG+AP+ N+       ++FEP+HGSA DI GKG+ANP A   +
Sbjct: 240 NLHADILSDLAAALSGSLGIAPTANLNPERLFPSMFEPIHGSAFDITGKGVANPIATFWT 299

Query: 281 AAMMLDYLGEKEAAKRVEKAVDLVLERGPRTPDLGGDATTEAFTEAVVEAL 331
           AAMML++LGEK AA+R+  A++ +   G  TPDLGG ATT + TEA+ + L
Sbjct: 300 AAMMLEHLGEKPAAERLMAAIEQITANGVFTPDLGGHATTASVTEAICKVL 350


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: 288
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: 358
Length adjustment: 29
Effective length of query: 305
Effective length of database: 329
Effective search space:   100345
Effective search space used:   100345
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 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