GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Pedobacter sp. GW460-11-11-14-LB5

Align histidinol-phosphate aminotransferase; tyrosine/phenylalanine aminotransferase (promiscuous) (EC 2.6.1.1; EC 2.6.1.9) (characterized)
to candidate CA265_RS03630 CA265_RS03630 histidinol-phosphate transaminase

Query= metacyc::BSU22620-MONOMER
         (360 letters)



>FitnessBrowser__Pedo557:CA265_RS03630
          Length = 346

 Score =  180 bits (457), Expect = 4e-50
 Identities = 115/358 (32%), Positives = 191/358 (53%), Gaps = 25/358 (6%)

Query: 3   IKEHLKQLKPYQPGKPIEAVKSEYGLDKVVKLASNENPYGCSEAAKEALHHEIQQLALYP 62
           ++E++K L+PY         + E+     V L +NEN YG    A             YP
Sbjct: 7   VRENIKNLRPYS------TARDEFKGQASVFLDANENSYGSPLPAN---------YNRYP 51

Query: 63  DGYSAALRTRLSKHLNVSETSLIFGNGSDEIIQIICRAFLND-KTNTVTAAPTFPQYKHN 121
           D     L+  +SK   V   +   GNGSDE I ++ RAF N  K N +   PT+  Y+ +
Sbjct: 52  DPLQLDLKDAISKIKGVPIENTFLGNGSDEAIDLLFRAFCNPGKDNVIVLPPTYGMYEVS 111

Query: 122 AVIEGAEVREIALRPDGSHDLDAMLEAIDEQTQVVWICSPNNPTGTYTSEGELLAFLERV 181
           A I   E+R+++L P+   D++ + E ID+ T++++ICSPNNPTG   +  ++   L   
Sbjct: 112 ANINDVEIRKVSLLPNFQLDMEKIAETIDKNTKLIFICSPNNPTGNSINREDIETILANF 171

Query: 182 PSRVLVVLDEAYYEYVTAEDYPETVPLLSKYSNLMILRTFSKAYGLAALRVGYGIADENL 241
               +VV+DEAY  Y   + +   +  L++Y NL++L+TFSKA+GLAALR+G   +   +
Sbjct: 172 NG--IVVVDEAYINYARQKTF---IQELTEYGNLVVLQTFSKAWGLAALRLGMAFSSTKV 226

Query: 242 IRQIEPAREPFNTSRLGQAAAIAALDDQAFIASCVEQNNAGLQQYYDFAKTHGL--KCYP 299
           I  +   + P+N ++  Q  A  AL + A +   ++++ A   +         +  K YP
Sbjct: 227 IDVLNKIKPPYNINQATQDLAFEALKNIAQVNDWIKESVAERDRLSKALTALNIVKKVYP 286

Query: 300 SQTNFVLIDFKRPADELFQALLEKGYIVRSGNALGF-PTSLRITIGTKEQNEEILAIL 356
           S  NF+L +    A +++  L+++G IVR  + +      LRIT+GTKE+N+++L +L
Sbjct: 287 SDANFILTEV-TDALKIYDTLVDQGIIVRDRSKVTLCEGCLRITVGTKEENDKLLTVL 343


Lambda     K      H
   0.317    0.134    0.382 

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: 296
Number of extensions: 20
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: 360
Length of database: 346
Length adjustment: 29
Effective length of query: 331
Effective length of database: 317
Effective search space:   104927
Effective search space used:   104927
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: 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