GapMind for Amino acid biosynthesis

 

Alignments for a candidate for asp-kinase in Sulfurivirga caldicuralii DSM 17737

Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate WP_074201259.1 BUQ81_RS04880 homoserine dehydrogenase

Query= BRENDA::Q9WZ17
         (739 letters)



>NCBI__GCF_900141795.1:WP_074201259.1
          Length = 434

 Score =  191 bits (485), Expect = 7e-53
 Identities = 120/319 (37%), Positives = 186/319 (58%), Gaps = 7/319 (2%)

Query: 17  VRKVRVGIAGLGTVGGSIYRILKERGNEIEKRIGEKFIISKVINRSPQKYELLGVPKEEI 76
           ++ +++G+ GLGTVGG    IL++  + +++R+     +S +  R   K   +     ++
Sbjct: 1   MKTIKLGLIGLGTVGGGTLAILRDSADLLQQRVNANIEVSIIAVRDLNKPRAVDTGSIQL 60

Query: 77  AFDFDDLILNSDV--VVEAIGGTDVAVDLVRRALELGRIVVTPNKNLISEYGNEFSEYIK 134
             D   ++ + DV  VVE +GGT +A +LV RA++ G+ VVT NK L++E+G+E     +
Sbjct: 61  TDDPTQVVNHPDVDIVVELMGGTGLARELVLRAIDNGKHVVTANKALLAEHGDEVFAAAE 120

Query: 135 KR--KLFFEASVGGGIPIISLLQDYLIFQKVTRIRGIMNGTTNYILTEMSK-GRHFEEVL 191
           K+  ++ +EA+  GGIPII  L++ L    +  + GI+NGT NYILTEM + G  F  VL
Sbjct: 121 KQGVQVAYEAAAAGGIPIIKALREGLSANNIDWVAGIINGTGNYILTEMKQPGADFNAVL 180

Query: 192 KEAQELGYAEADPTNDIEGYDVAYKVSVLAGVVTGRFPGINSVQFEGITRIDPEYLKEIV 251
           K AQELGYAEADPT D+EG D A+K+++LA +  G       V  EGI+RI  + ++   
Sbjct: 181 KRAQELGYAEADPTFDVEGIDAAHKLTILASLAFGIPLQFEKVYTEGISRISADDMRFAD 240

Query: 252 RSGKKLKLIGELDFSTNRYEVRLR-EVTPEDPFF-NVDGVDNAIEVSTDLAGDFLLKGRG 309
             G ++K +G    + +   +R+   + P+     NV GV NA+    D  G  L  G G
Sbjct: 241 MLGYEIKHLGIARRTDDGVSMRVHPTLIPKSVLLANVSGVMNAVMTHGDHVGPTLYYGPG 300

Query: 310 AGGYPTASAVIADLFRVAK 328
           AG  PTASAV+AD+  V +
Sbjct: 301 AGAGPTASAVVADIVDVVR 319


Lambda     K      H
   0.318    0.137    0.377 

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: 714
Number of extensions: 34
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: 739
Length of database: 434
Length adjustment: 36
Effective length of query: 703
Effective length of database: 398
Effective search space:   279794
Effective search space used:   279794
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: 53 (25.0 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