GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Caldicellulosiruptor kronotskyensis 2002

Align histidinol-phosphate aminotransferase; tyrosine/phenylalanine aminotransferase (promiscuous) (EC 2.6.1.1; EC 2.6.1.9) (characterized)
to candidate WP_013430740.1 CALKRO_RS09110 histidinol-phosphate transaminase

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



>NCBI__GCF_000166775.1:WP_013430740.1
          Length = 358

 Score =  313 bits (801), Expect = 6e-90
 Identities = 160/357 (44%), Positives = 223/357 (62%), Gaps = 1/357 (0%)

Query: 4   KEHLKQLKPYQPGKPIEAVKSEYGLDKVVKLASNENPYGCSEAAKEALHHEIQQLALYPD 63
           +E +  + PY PGKPI  VK E GL+KV+KLASNENP G SE  K+AL   + +L +YPD
Sbjct: 3   REVINTISPYIPGKPISEVKRELGLEKVIKLASNENPLGPSENVKKALMQNLDELGIYPD 62

Query: 64  GYSAALRTRLSKHLNVSETSLIFGNGSDEIIQIICRAFLNDKTNTVTAAPTFPQYKHNAV 123
           G    L+ +LSK L V  + ++ G GSDEI Q I   F+N   N + A P+FP+Y+    
Sbjct: 63  GNCTELKLKLSKKLGVKPSQILLGAGSDEITQFIAAVFINPGDNAIMAKPSFPRYETVTK 122

Query: 124 IEGAEVREIALRPDGSHDLDAMLEAIDEQTQVVWICSPNNPTGTYTSEGELLAFLERVPS 183
           + G    E+ L+ D +HDL+A    I+E+T+V+WIC+PNNPTGT     EL  F++ VPS
Sbjct: 123 VMGGIPIELPLK-DFTHDLEAFYNNINERTKVIWICNPNNPTGTIVKRKELYDFIKSVPS 181

Query: 184 RVLVVLDEAYYEYVTAEDYPETVPLLSKYSNLMILRTFSKAYGLAALRVGYGIADENLIR 243
            + VV+D+AY EY+   +YP+    L ++ NL++L+TFSK YGLA+LR+GY IA E +I 
Sbjct: 182 HIAVVVDQAYKEYIDDPEYPDATEWLYEFENLIVLQTFSKIYGLASLRIGYAIASEEIIE 241

Query: 244 QIEPAREPFNTSRLGQAAAIAALDDQAFIASCVEQNNAGLQQYYDFAKTHGLKCYPSQTN 303
           ++   R PFN + L Q AA AALDD+  +    E N   L+ +Y   +  GL    S  N
Sbjct: 242 KLNRVRPPFNVNHLAQIAASAALDDEEHVKKAKELNKKSLEFFYKNFEEMGLFYIKSYGN 301

Query: 304 FVLIDFKRPADELFQALLEKGYIVRSGNALGFPTSLRITIGTKEQNEEILAILAEIL 360
           FV++D K+ A ++F+ LL KG IVR G+  G PT LR+T G +  N   +  L EIL
Sbjct: 302 FVMVDVKKDAVDVFKKLLLKGIIVRPGDIFGMPTYLRVTTGQEGDNMGFIKALKEIL 358


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: 336
Number of extensions: 15
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: 360
Length of database: 358
Length adjustment: 29
Effective length of query: 331
Effective length of database: 329
Effective search space:   108899
Effective search space used:   108899
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 Jul 26 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