GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisC in Halomonas desiderata SP1

Align Histidinol-phosphate aminotransferase 1; EC 2.6.1.9; Imidazole acetol-phosphate transaminase 1 (uncharacterized)
to candidate WP_086509941.1 BZY95_RS10840 threonine-phosphate decarboxylase

Query= curated2:Q4FSH2
         (380 letters)



>NCBI__GCF_002151265.1:WP_086509941.1
          Length = 366

 Score =  152 bits (384), Expect = 1e-41
 Identities = 105/362 (29%), Positives = 187/362 (51%), Gaps = 20/362 (5%)

Query: 26  PYQTGKPIEELTREYGV---SDVVKLASNENPIGCSPHVTLAITEQIGQLSRYPDGNGYY 82
           P   G+P E+L   +G+   S+V+  ++N NP+G  P +   +   + +L+ YPD +   
Sbjct: 5   PSHGGRP-EQLLPRFGLAGDSEVIDFSANLNPLGPPPWLAQRLAACVTELAVYPDPDYCE 63

Query: 83  LKQALADFNDVNVDQITLGNGSDDLLDILARSFV--GADDAIVYSQYAFVVYSMLAKMQG 140
            + A+A    +   Q+ L NG  + + + A      G   A +  Q  F  Y    +  G
Sbjct: 64  ARDAIAMSEGLGPKQVRLTNGGAEAIFLAAALLARQGVRRAAIV-QPTFGEYERACRHYG 122

Query: 141 AM--DVEVPAQRFGHDLKAMSQAIENNSNTKIVFIANPNNPTGTQLEHGELREFVASVPS 198
                VE+    F  D     +A+ +      +F+  PNNPTGT +E G +   +A+  S
Sbjct: 123 IAVEHVELAPGSFALDEARADEAMRD---VGALFLCRPNNPTGTLIERGVVERLLATGRS 179

Query: 199 -SVLVVLDEAYIEY-SPESNNRALLDEFDNVVIVRTFSKAYGLAGLRVGYALSSAAVADL 256
              ++V+DEA++++ +P+     LL  FDN++++R+ +K Y + GLR+GY L SAA  + 
Sbjct: 180 HGAMLVVDEAFVDFVTPDERLTPLLARFDNLLLLRSMTKLYAIPGLRLGYLLGSAAAVNA 239

Query: 257 LNRIRQPFNVSRVALAAAAAALADQDFIEKTRLINDEQMHWLEKQFDALGLGFIKSHANF 316
           +  ++ P++V+ +A    A  LAD+D++ +TR   D +  WL+ +  ALGL  + SHANF
Sbjct: 240 IAELQPPWSVNALAAGLVAPLLADRDYLARTRAWLDAERPWLQGELAALGLDVVPSHANF 299

Query: 317 IMVEIAVEMEDTNAA---VIYQALLEQGVIVRQLEVY-GLYN-WLRISVGVAEDNMRLID 371
           ++   A  ++D        + + L   G++VR    + GL   WLR++V    +N  L++
Sbjct: 300 LLFRDA-RLQDARGGSMPALLEHLARGGILVRHTHHFIGLEGAWLRVAVRSRPENRALVE 358

Query: 372 TL 373
            +
Sbjct: 359 AI 360


Lambda     K      H
   0.318    0.134    0.372 

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: 265
Number of extensions: 11
Number of successful extensions: 3
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: 380
Length of database: 366
Length adjustment: 30
Effective length of query: 350
Effective length of database: 336
Effective search space:   117600
Effective search space used:   117600
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