GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hcs in Desulfovibrio vulgaris Miyazaki F

Align homocitrate synthase (EC 2.3.3.14) (characterized)
to candidate 8501897 DvMF_2612 pyruvate carboxyltransferase (RefSeq)

Query= BRENDA::A0A1Y6KBA1
         (416 letters)



>FitnessBrowser__Miya:8501897
          Length = 455

 Score =  221 bits (562), Expect = 5e-62
 Identities = 140/377 (37%), Positives = 209/377 (55%), Gaps = 19/377 (5%)

Query: 42  ILNDTTLRDGEQAPGVAFALSEKVAIARALARAGVPEIEAGTPAM-GADEISAIRAIVEA 100
           +L DTTLR+GEQ+ G   +++++  + R LA  GVPE E G        ++ A+ A V  
Sbjct: 1   MLLDTTLREGEQSFGTYLSMADRERVLRGLAAVGVPEAEVGWAGREDLTDMLALSARVAP 60

Query: 101 GLPATIIGWCRMREADVDAAIAAGVSMVNVSIPTSDVQIAAKLGGGRSVALELLKRVVSY 160
           GL A    WCR R  D+ AA+A G S V V +P SD  +A +LG GR+  L+LL   ++ 
Sbjct: 61  GLAAA--AWCRCRPGDLRAAVACGASRVCVGVPVSDAHLARRLGLGRAALLDLLAATLAE 118

Query: 161 ARSRGLG-VAVGGEDSSRADVGFLAEVIATAKALGARRFRVADTLSVLDPDATSALVGAL 219
           AR  G+  V VG ED+SRAD  F+  V   A A GA R R++DT+ +  P   + +V AL
Sbjct: 119 ARMLGIEHVTVGMEDASRADRAFVFAVACHAAAHGAHRVRLSDTVGLYTPLEVADVVRAL 178

Query: 220 RATTD-------------LEIEFHGHDDLGLATANTLAAIKAGATHASVTVIGLGERAGN 266
           RA  +             + I  H H+D G+ATAN L A++ GA  A V+V+GLGERAG 
Sbjct: 179 RAELEGARQDDTAPRARRVSIGTHFHNDCGMATANALTALECGADCADVSVLGLGERAGV 238

Query: 267 APLEEVAVALRQLYRRETGIVLAELDHVANVVAAAAARAIPLNKAIVGEHVFTHESGIHV 326
           A LEE+A AL  + R      LA L  +   VA AA+ ++P +  + G  +F  ESG+H 
Sbjct: 239 ARLEELAAAL--VVRGRARFELAPLRALCGQVAQAASLSVPRHWPVAGRDIFAVESGLHA 296

Query: 327 DGLLKDQRTYQALDPMLFGRSNRIVIGKHSGLSAITSLLSDLRLPASADQAQRILARVRK 386
            G+ +D   ++   P L G S R+ +G+ SG++A+ + L++L +    D+   I+  VR 
Sbjct: 297 HGVRRDPSLFEPFPPELVGDSRRMGVGRKSGVAAVAAALAELSILPPPDELPAIVEAVRD 356

Query: 387 HAVAHKGPVPKEAVAAI 403
            +   + P+    +A +
Sbjct: 357 LSATLRRPLTPAELAEV 373


Lambda     K      H
   0.317    0.132    0.369 

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: 523
Number of extensions: 30
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: 416
Length of database: 455
Length adjustment: 32
Effective length of query: 384
Effective length of database: 423
Effective search space:   162432
Effective search space used:   162432
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 (21.7 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 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