GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Thermocrinis albus DSM 14484

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_012991633.1 THAL_RS02960 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000025605.1:WP_012991633.1
          Length = 361

 Score =  236 bits (602), Expect = 6e-67
 Identities = 154/362 (42%), Positives = 210/362 (58%), Gaps = 36/362 (9%)

Query: 3   YRICLIEGDGIGHEVIPAARRVL----EATGLPLEFVEAEAGWETFERRGTSVPEETVEK 58
           ++I ++EGDGIG EV+ AA +VL    E  G   E  +   G    + +GT +PEET++ 
Sbjct: 4   FKIAVLEGDGIGPEVVSAALKVLYRIGELAGHHFETEKGLIGGSAIDEKGTPLPEETIKL 63

Query: 59  ILSCHATLFGAATSPT--------RKVPGFFGAIRYLRRRLDLYANVRPAKS-RPVPGSR 109
            L   A L GA   P         R   G  G    +R+ LDLYAN+RPAK   P+  + 
Sbjct: 64  CLEADAVLLGAVGGPKWDHLPTEERPERGLLG----IRKALDLYANLRPAKVYEPLIEAS 119

Query: 110 P-------GVDLVIVRENTEGLYVEQERRYLD-----VAIADAVISKKASERIGRAALRI 157
           P       G D+V+VRE T  +Y  + R         V I     ++    R+ R A +I
Sbjct: 120 PLKREVVRGTDMVVVRELTGDVYYGEPRGIFTQDGKRVGINTMRYTEDEIRRVVRKAFQI 179

Query: 158 AEGRPRKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERF 217
           A  R RK L    K+NVL ++  L+   V+E +K+FP V ++ + VDNCAMQ+V RP  F
Sbjct: 180 ANLR-RKKLTSVDKSNVLEVS-ALWRQIVEEESKNFPEVELEHLYVDNCAMQIVRRPSSF 237

Query: 218 DVIVTTNLLGDILSDLAAGLVGGLGLAPSGNIGDTTAVFEPVHGSAPDIAGKGIANPTAA 277
           DVIVT N+ GDILSD AA + G LG+ PS ++GD  A++EPVHGSAPDIAGKG+ANP A 
Sbjct: 238 DVIVTGNIFGDILSDEAAVITGSLGMLPSASLGDRYALYEPVHGSAPDIAGKGVANPIAT 297

Query: 278 ILSAAMMLDY-LGEKEAAKRVEKAVDLVLERGPRTPDLGGDAT----TEAFTEAVVEALK 332
           ILS A+ML Y  G    A  +E+AV++ LE+G RTPD+  + T    TE  T+AV++ L+
Sbjct: 298 ILSVALMLRYSFGLIREADLLERAVEVTLEKGYRTPDIYTEGTIKVGTEGMTQAVIQTLE 357

Query: 333 SL 334
            L
Sbjct: 358 EL 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: 343
Number of extensions: 24
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: 361
Length adjustment: 29
Effective length of query: 305
Effective length of database: 332
Effective search space:   101260
Effective search space used:   101260
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 Jul 25 2024. The underlying query database was built on Jul 25 2024.

Links

Downloads

Related tools

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