GapMind for Amino acid biosynthesis

 

Alignments for a candidate for asp-kinase in Methanobacterium lacus AL-21

Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate WP_013643891.1 METBO_RS01460 homoserine dehydrogenase

Query= BRENDA::Q9WZ17
         (739 letters)



>NCBI__GCF_000191585.1:WP_013643891.1
          Length = 426

 Score =  188 bits (478), Expect = 4e-52
 Identities = 129/365 (35%), Positives = 209/365 (57%), Gaps = 21/365 (5%)

Query: 20  VRVGIAGLGTVGGSIYRILKERGNEIEKRIGEKFIISKVINRSPQKYELLGVPKEEIAFD 79
           V +G+ G GT+G  +   L +  + +E ++G+K  + KV++        + +  + ++ D
Sbjct: 5   VNIGLIGFGTIGSGVVETLNKNIDLVENKVGKKVKLKKVVDLDITTDRGVEISSDVLSTD 64

Query: 80  FDDLILNSDV--VVEAIGGTDVAVDLVRRALELGRIVVTPNKNLISEYGNEFSEYIKKR- 136
            +D++ + D+  V+E +GG   A+  + +A+E G+ VVT NK L++++ +E     +K  
Sbjct: 65  INDILDDPDIEIVIELMGGYQPALKFITKAMENGKHVVTANKALLAKHWDEIISTAQKND 124

Query: 137 -KLFFEASVGGGIPIISLLQDYLIFQKVTRIRGIMNGTTNYILTEMS-KGRHFEEVLKEA 194
            ++ FEASVGGGIP++  L + L    +  I GI+NGT NYILT+M+ +G  FE+VLKEA
Sbjct: 125 VRICFEASVGGGIPLLQPLNEGLSANNIQSIYGIINGTANYILTKMTDEGLEFEDVLKEA 184

Query: 195 QELGYAEADPTNDIEGYDVAYKVSVLAGVVTGRFPGINSVQFEGITRIDPE---YLKEIV 251
           Q+ GYAEADP+ DIEG D A K+ +L  +  G++   ++   EGIT I PE   + KE +
Sbjct: 185 QKKGYAEADPSFDIEGDDTAQKLIILTILSFGKYIKQDNFHVEGITCITPEDISFAKEEL 244

Query: 252 RSGKKLKLIGELDFSTNRYEVRLR-EVTPEDPFF-NVDGVDNAIEVSTDLAGDFLLKGRG 309
            S  KL  I +L     + EVR+   + P D    +V+GV N + +  D+ G  ++ G G
Sbjct: 245 NSCIKLLAIAKL--VDGKLEVRVHPTIVPLDHLLSSVNGVFNGVYLVGDVVGPVMMYGPG 302

Query: 310 AGGYPTASAVIADLFRV---AKYKVLGGAEKFSVVVMKFGGAAISDVEKLEKVAEKIIKR 366
           AG  PTASAV+ D   +    +  VL G +  +V  +K     ISD+E   K   ++I +
Sbjct: 303 AGMMPTASAVVGDCIDIIENMEKPVLYGPKSCTVEKIK----DISDLE--SKYYLRLITK 356

Query: 367 KKSGV 371
            + GV
Sbjct: 357 DEPGV 361


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: 760
Number of extensions: 43
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: 426
Length adjustment: 36
Effective length of query: 703
Effective length of database: 390
Effective search space:   274170
Effective search space used:   274170
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