GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hcs in Desulfovibrio bastinii DSM 16055

Align Homocitrate synthase 1; EC 2.3.3.14 (uncharacterized)
to candidate WP_027177793.1 G496_RS0101950 pyruvate carboxyltransferase

Query= curated2:Q44290
         (377 letters)



>NCBI__GCF_000429985.1:WP_027177793.1
          Length = 368

 Score =  217 bits (553), Expect = 4e-61
 Identities = 133/371 (35%), Positives = 207/371 (55%), Gaps = 5/371 (1%)

Query: 5   LINDTTLRDGEQAAGVVFTLEEKVAIAKFLDTIGVPELEVGIPAMGEEEMRAICA-ISNL 63
           ++ DTTLR+G Q  G  F L  +  IA  L  +G+ E+E+G   +G++ +  +   I ++
Sbjct: 1   MLIDTTLREGAQLFGAYFNLSTRKKIAAGLAEVGIDEIELGW--IGQDNLGTLAEYIKDI 58

Query: 64  GLKANLLAWNRAVISDIKASVACGMERVHIAIPVSGIQIAAKFHGQWRVSLQRLKDCISF 123
                L  W     +DI  +    ++RV+I +PVS + I  +        L RL   I  
Sbjct: 59  SKDTYLSVWTPCREADIMKASKLPIDRVNIGVPVSDLHIEERLGLDRNGLLHRLSSAIRT 118

Query: 124 AVDQGL-WVAVGGEDSSRADENFLLDVALYAQEWGASRFRFCDTVGVLDPFTTYGKVKLL 182
           A   G+ +V+VG ED SRAD +F L VA +A+  GASR R  D++G L P +    ++  
Sbjct: 119 AKAFGIEYVSVGMEDVSRADPDFALTVAAHAKNCGASRIRLSDSLGQLTPKSMEKLIETF 178

Query: 183 VSALTIPVEVHTHNDFGMATANALAGIKAGASSVNTTVIGLGERAGNAALEEVVMAIKRI 242
            + + I   VH H+DFGMATANA+  ++ GA   + +V+G+GER+G AA EE+   +   
Sbjct: 179 RNHVKIDTAVHCHDDFGMATANAVTALECGADYADVSVLGIGERSGIAATEELAAYLALR 238

Query: 243 YGVDMGIDTPRLLELSQLVAAASGANVPPWKAIVGENTFAHESGIHAHGVLQNPDTYEPF 302
            G      T ++  L  +VA  +G  VP  KA+VGE+ FA ESG+H H + ++P+ +EP+
Sbjct: 239 CG-KKRYSTQKIKALCSMVALEAGVVVPRTKAVVGEDIFACESGLHTHALSKSPELFEPY 297

Query: 303 APEEVGWERRLVVGKHSGRHSVSNLLEQHGIFLNPEETQSVLDAVRQQSIKKKRSLTTEE 362
            PE VG  R+L VG  SG+ +V + L+  G+  +P++  ++  AVRQ S + KR LT  E
Sbjct: 298 QPESVGISRKLAVGGKSGKAAVKSALKDCGVENDPKDITALTMAVRQLSSRLKRPLTRSE 357

Query: 363 LLNLVKEQRYS 373
            + L   +  S
Sbjct: 358 FIKLSSGEHLS 368


Lambda     K      H
   0.318    0.133    0.388 

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: 338
Number of extensions: 10
Number of successful extensions: 4
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: 377
Length of database: 368
Length adjustment: 30
Effective length of query: 347
Effective length of database: 338
Effective search space:   117286
Effective search space used:   117286
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: 50 (23.9 bits)

This GapMind analysis is from Apr 10 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