GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Nitratiruptor tergarcus DSM 16512

Align histidinol-phosphate aminotransferase; tyrosine/phenylalanine aminotransferase (promiscuous) (EC 2.6.1.1; EC 2.6.1.9) (characterized)
to candidate WP_084275315.1 B8779_RS04270 histidinol-phosphate transaminase

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



>NCBI__GCF_900176045.1:WP_084275315.1
          Length = 368

 Score =  242 bits (618), Expect = 1e-68
 Identities = 145/358 (40%), Positives = 210/358 (58%), Gaps = 15/358 (4%)

Query: 1   MRIKEHLKQLKPYQPGKPIEAVKSEYGLDK--VVKLASNENPYGCSEAAKEALHHEIQQL 58
           MR  E+L++LK Y+ GKPIE V  EYG+D+  ++KLASNENPYG S    + +     ++
Sbjct: 1   MRFNENLQRLKTYEAGKPIELVVREYGIDEKDIIKLASNENPYGTSPKVVKKVQENAHKM 60

Query: 59  ALYPDGYSAALRTRLSKHLNVSETSLIFGNGSDEIIQIICRAFLNDKTNTVTAAPTFPQY 118
            LYPD     L+  L+K   VS   +I G GSD++++   RA LN+ T+ + +  TF  Y
Sbjct: 61  YLYPDDSMYELKAALAKRFGVSAEEIIIGAGSDQVLEFCARAVLNEHTSVLMSKITFAMY 120

Query: 119 KHNAVIEGAEV-REIALRPDGSHDLDAMLEAIDEQT-QVVWICSPNNPTGTYTSEGELLA 176
           +  A+ +G+++ R    R    HDLD   +   +    +V IC+PNNPTG    +  L +
Sbjct: 121 EIYALQQGSKIIRSSCYR----HDLDEFYDLYQKHNPSIVHICTPNNPTGDAIDKEYLYS 176

Query: 177 FLERVPSRVLVVLDEAYYEYVTAEDYPETVP---LLSKYSNLMILRTFSKAYGLAALRVG 233
           FLE+V    LVV+D AY EY   +D  + +P   L++ Y N + L TFSKAYGL  +RVG
Sbjct: 177 FLEKVKDP-LVVVDGAYMEYAAYKDPKKLIPPRELIAMYPNAIYLGTFSKAYGLGGMRVG 235

Query: 234 YGIADENLIRQIEPAREPFNTSRLGQAAAIAALDDQAFIASCVEQNNAGLQQYYDFAKTH 293
           YGIA + +I+Q+   R PFN + L   AA  AL D+ F+   +E+N A + ++  FA  +
Sbjct: 236 YGIAQKEIIQQLYKLRPPFNITTLSLLAATEALKDEEFVQRAIEKNFAQMDRFIHFAMQN 295

Query: 294 GLKCYPSQTNFV--LIDFKRPADELFQALLEKGYIVRSGNALGFPTSLRITIGTKEQN 349
            L+   S TNF+  L+     A +L  ALL +G IVR  ++ G   +LRITIGT EQN
Sbjct: 296 ELEFIDSYTNFITYLLPQNINAKDLANALLRRGIIVRDLSSYGM-NALRITIGTPEQN 352


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: 374
Number of extensions: 19
Number of successful extensions: 8
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 360
Length of database: 368
Length adjustment: 29
Effective length of query: 331
Effective length of database: 339
Effective search space:   112209
Effective search space used:   112209
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 10 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