GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisC in Anaerobutyricum hallii DSM 3353

Align Histidinol-phosphate aminotransferase; EC 2.6.1.9; Imidazole acetol-phosphate transaminase (uncharacterized)
to candidate WP_005345775.1 EUBHAL_RS05010 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= curated2:A9AA96
         (371 letters)



>NCBI__GCF_000173975.1:WP_005345775.1
          Length = 391

 Score =  107 bits (267), Expect = 6e-28
 Identities = 91/307 (29%), Positives = 146/307 (47%), Gaps = 22/307 (7%)

Query: 81  KFTKMPVENIIVGGDGADEVIDNIMRILIDEDDEVIIPIPTFTQYAISAKIHGANIKWAK 140
           + T  P   I+V   G+ E ID  +R +++  DEVI+P P F  Y    K+         
Sbjct: 83  ELTYNPAHEIVVTVGGS-EGIDLALRAMLNPGDEVILPEPAFVSYLPCVKLADGVPVTID 141

Query: 141 FDEENGFKLDAESVLNNITEKTKAIFLCTPNNPTGNVIPTED---IKKIVESTDALVMID 197
             EEN FKL  E +L  IT+KTK + L  PNNPTG ++  ED   I +IV+  D  V+ D
Sbjct: 142 LKEENHFKLKPEELLAVITDKTKILILSYPNNPTGAIMTREDLEPIAEIVKEKDLYVISD 201

Query: 198 HAYIE--YSKEEYDLTNWALKYDNVLVLRTFSKVFGLAGQRVGYGVTSKKLVDYMMRIK- 254
             Y E  Y ++   + +     D  +++  FSK F + G R+G+    + ++  +++I  
Sbjct: 202 EIYAELTYGQDHCSIASLPGMRDRTIIINGFSKSFAMTGWRMGFATGPELIMQQILKIHQ 261

Query: 255 -PIFSLTRASQVSAITALQDKEFFKKCLKEGIESRE----EIYN--GLKKFKQLEVYPTE 307
             I +    SQ +AI A+ + E   + ++     R     E+++  GLK F+     P  
Sbjct: 262 FAIMAAPTTSQYAAIEAMTNGEEDVQIMRNAYNQRRRFVLELFSEMGLKCFE-----PEG 316

Query: 308 ANYMLVKVKN-GMNSSEFCEALLK-KGVIVRDCYSFEGLEPYYFRVSIG-TFEENERFLK 364
           A Y+   +K  GM S EF    L+ + V +    +F      + RVS   + EE +  L 
Sbjct: 317 AFYIFPCIKEFGMTSDEFANRFLREEKVAIIPGTAFGDCGEGFLRVSYAYSIEELKEALG 376

Query: 365 IMSEIVE 371
            ++  VE
Sbjct: 377 RLANFVE 383


Lambda     K      H
   0.317    0.136    0.389 

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: 344
Number of extensions: 20
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: 371
Length of database: 391
Length adjustment: 30
Effective length of query: 341
Effective length of database: 361
Effective search space:   123101
Effective search space used:   123101
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 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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