GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cmutase in Desulfuromonas acetexigens

Align 3-deoxy-7-phosphoheptulonate synthase (EC 2.5.1.54); chorismate mutase (EC 5.4.99.5) (characterized)
to candidate WP_092054776.1 BQ4888_RS05610 3-deoxy-7-phosphoheptulonate synthase

Query= BRENDA::P39912
         (358 letters)



>NCBI__GCF_900111775.1:WP_092054776.1
          Length = 336

 Score =  278 bits (712), Expect = 1e-79
 Identities = 152/327 (46%), Positives = 212/327 (64%), Gaps = 10/327 (3%)

Query: 31  VKEIGKAKEAQGVNRFD-PVRERTMLNNIIENNDGPFENSTIQHIFKEIFKAGLELQEED 89
           ++ + KA EA G+     P  ERT +   +  N G  ++STI+ +       G+      
Sbjct: 14  IRSVEKAVEAMGLQASPIPGSERTAIG--VLGNQGYVDDSTIREL------PGVVECIHV 65

Query: 90  HSKALLVSRKKKPEDTIVDIKGEKIGDGQQRFIV-GPCAVESYEQVAEVAAAAKKQGIKI 148
                LVSR   PE TIV++   KIG+G    ++ GPC++ES  Q+   A   K  G +I
Sbjct: 66  SKPYKLVSRDFHPEPTIVEVGPVKIGNGLPPVVMAGPCSIESEAQMLASARVVKAAGAQI 125

Query: 149 LRGGAFKPRTSPYDFQGLGVEGLQILKRVADEFDLAVISEIVTPAHIEEALDYIDVIQIG 208
           LRGGAFKPRT P+ FQGLGVEGL+ L+R  DE  L V++E++    +++   Y D++QIG
Sbjct: 126 LRGGAFKPRTGPHSFQGLGVEGLKYLRRAGDEAGLPVVTEVMRIEQLDDVCRYADILQIG 185

Query: 209 ARNMQNFELLKAAGAVKKPVLLKRGLAATISEFINAAEYIMSQGNDQIILCERGIRTYET 268
           ARNMQNF+LLK  G  + PVLLKRG++AT+ EF+ AAEYI+++GN Q+ILCERGIRT+E 
Sbjct: 186 ARNMQNFDLLKEVGKRRHPVLLKRGMSATLEEFLAAAEYIVAEGNGQVILCERGIRTFEK 245

Query: 269 ATRNTLDISAVPILKQETHLPVFVDVTHSTGRRDLLLPTAKAALAIGADGVMAEVHPDPS 328
           ATRNTLD+S VP++++ +HLP+ VD +H+TG R L+   +KAAL  GA G+M EVHP+P 
Sbjct: 246 ATRNTLDLSIVPLIRKMSHLPIIVDPSHATGIRALVPVMSKAALVAGAHGLMVEVHPEPE 305

Query: 329 VALSDSAQQMAIPEFEKWLNELKPMVK 355
            AL D AQ +    F   + EL  ++K
Sbjct: 306 KALCDGAQSLTGEGFATLMGELSGLLK 332


Lambda     K      H
   0.316    0.134    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: 325
Number of extensions: 18
Number of successful extensions: 2
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: 358
Length of database: 336
Length adjustment: 29
Effective length of query: 329
Effective length of database: 307
Effective search space:   101003
Effective search space used:   101003
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 (21.6 bits)
S2: 49 (23.5 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