GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisC in Phaeobacter inhibens BS107

Align Histidinol-phosphate aminotransferase; EC 2.6.1.9; Imidazole acetol-phosphate transaminase (uncharacterized)
to candidate GFF2362 PGA1_c23930 putative histidinol-phosphate aminotransferase

Query= curated2:A7HCR6
         (364 letters)



>FitnessBrowser__Phaeo:GFF2362
          Length = 369

 Score =  178 bits (452), Expect = 2e-49
 Identities = 120/333 (36%), Positives = 169/333 (50%), Gaps = 9/333 (2%)

Query: 2   PLVPPHVASLTPYVPGKPIEEVEREYGVSNVAKLASNENALGPSPLALAAAREACAKVHL 61
           P   P   SL   VP    E  ER+ G    A+L +NEN  GPSP A+AA + +  ++  
Sbjct: 4   PRYTPLAQSLPASVPFVGPETQERQRGAPFAARLGANENIFGPSPKAIAAMQGSLGEIWK 63

Query: 62  YPDGSAYLLRNAIAAKLGVPPEEVMVGNGSNELIELLVRTFVLDGEEVLTSAQSFVAYKL 121
           Y D  ++ LR A+AA   V PE +M+G G + L+  LVR  + +G+ V+TS  ++  +  
Sbjct: 64  YGDAESHDLRAALAAHHSVAPENIMIGEGIDGLLGYLVRLLIGEGDAVVTSLGAYPTFNY 123

Query: 122 AAHEHGRTLVEAPMKGRFHYDLDALRKLLSRRTKLVFLANPDNPTGTWFTEAELTPFLDA 181
                G  L   P +           K      KLV+LANPDNP G+W + A L   +DA
Sbjct: 124 HVAGFGGVLHTVPYQDDHEDPAALFAKAAEVDAKLVYLANPDNPMGSWHSGAGLLAAMDA 183

Query: 182 VPKDTLVVLDEAYVEYVDAPGFQDGLALRRKY--PNVVVLRTFSKIYGLAGMRLGYGLAR 239
           +P+  L++LDEAY++   AP   DG AL      P V+  RTFSK YG+AG R+GY LA 
Sbjct: 184 LPEGCLLLLDEAYIDC--AP---DGTALPIDINDPRVIRTRTFSKAYGMAGARVGYVLAE 238

Query: 240 PEVVEYVDRVRPPFNTNLVAQAAGAAALGDSAHVAKSRALVLEERPFLAKGLAALGAIVV 299
             ++   ++VR  F  N  AQ    AAL D A +A+    +   R  +A+     G   +
Sbjct: 239 AGLISAFNKVRNHFGMNRTAQIGALAALRDQAWLAEVLGRIATARNRIAQIARDNGLTPL 298

Query: 300 PSQGNFVLAD--FPGRTGKDLFEALLREGVIAR 330
           PS  NFV  D    G   K + E L+ +GV  R
Sbjct: 299 PSATNFVAIDCGADGAFAKSVLEGLVDQGVFVR 331


Lambda     K      H
   0.320    0.138    0.399 

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: 332
Number of extensions: 13
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: 364
Length of database: 369
Length adjustment: 30
Effective length of query: 334
Effective length of database: 339
Effective search space:   113226
Effective search space used:   113226
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 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