GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisC in Caulobacter crescentus NA1000

Align Histidinol-phosphate aminotransferase; EC 2.6.1.9; Imidazole acetol-phosphate transaminase (uncharacterized)
to candidate CCNA_01124 CCNA_01124 histidinol-phosphate aminotransferase

Query= curated2:A7HCR6
         (364 letters)



>FitnessBrowser__Caulo:CCNA_01124
          Length = 347

 Score =  130 bits (326), Expect = 7e-35
 Identities = 101/322 (31%), Positives = 164/322 (50%), Gaps = 21/322 (6%)

Query: 37  SNENALGPSPLAL-AAAREACAKVHLYPDGSAYLLRNAIAAKLGVPPEEVMVGNGSNELI 95
           +NEN LGPS  A  A AR A         G   LL   IAA+ G+ PE + V  GS+E +
Sbjct: 5   ANENPLGPSKAACDAIARVAPLGGRYDLTGETELLTKTIAAQSGLKPEFIAVYAGSSEPL 64

Query: 96  ELLVRTFVLDGEEVLTSAQSFVAYKLAAHEHGRTLVEAPMKGRFHYDLDALRKLLSRRTK 155
              V  F    +  +T+  S+ A   AA      +++ P+   F +D+ A+      +  
Sbjct: 65  HYSVLAFTSPTKSFVTADPSYEAGMFAARTSQAKIIKTPLTSAFAHDVKAM-VAADAQAG 123

Query: 156 LVFLANPDNPTGTWFTEAELTPFLDAVPKDTLVVLDEAYVEYVDAPGFQDGLALRRKYPN 215
           ++++ NP+NPTGT  T+ ++   L+  P  +++++DEAY+   D P   D L L  +  +
Sbjct: 124 VIYICNPNNPTGTLTTKKDIVWALENKPAGSILLVDEAYIHLTDEP---DTLDLVAQGKD 180

Query: 216 VVVLRTFSKIYGLAGMRLGYGLARPEVVEYVDRVRPPFNTN---LVAQAAGAAALGDSAH 272
           ++VLRTFSKIYG+AG+R G+   RP+++  +     PF  N   +   AA  A+L D   
Sbjct: 181 LIVLRTFSKIYGMAGIRCGFAAGRPDLLAKL----KPFGQNAMPITGSAAARASLEDPKL 236

Query: 273 VAKSRALVLEERPFLAKGLAALG-AIVVPSQGNFVLADFPGRTGKDLFEAL-LREGVIAR 330
           V + R ++ + R      L   G  ++   Q N  + D  GR G+ +  A+  R  +I R
Sbjct: 237 VPERRKMIGDTRRDTIAWLKTNGYKVIGDPQTNCFMID-TGRNGRAVMAAMKARNVMIGR 295

Query: 331 --PVAGYGFPSALRITVGLRRE 350
             P+    +P+A+R++VG   E
Sbjct: 296 TWPI----WPNAVRVSVGTPEE 313


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: 272
Number of extensions: 10
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: 364
Length of database: 347
Length adjustment: 29
Effective length of query: 335
Effective length of database: 318
Effective search space:   106530
Effective search space used:   106530
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