GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tpiA in Polaromonas naphthalenivorans CJ2

Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate WP_011801377.1 PNAP_RS09960 phosphoglycerate kinase

Query= BRENDA::P36204
         (654 letters)



>NCBI__GCF_000015505.1:WP_011801377.1
          Length = 400

 Score =  295 bits (756), Expect = 2e-84
 Identities = 167/379 (44%), Positives = 241/379 (63%), Gaps = 13/379 (3%)

Query: 14  KRVIMRVDFNVPVK-DGVVQDDTRIRAALPTIKYALEQGAKVILLSHLGRP-KGEPSPEF 71
           KRV +R D NVP    G + +DTRIRA+LP I+ AL+ GA V++ SHLGRP +G   P  
Sbjct: 18  KRVFIRADLNVPQDASGRITEDTRIRASLPCIRMALDAGAAVMVTSHLGRPAEGGFKPGD 77

Query: 72  SLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRFHPGETKNDPELA 131
           SLAPVA+RLSELLG+ V  V + V D V      ++ G+++LLEN R + GE  ND  L+
Sbjct: 78  SLAPVAERLSELLGRPVSLVSSWV-DGVP-----VEPGQLVLLENCRLNAGEKSNDEALS 131

Query: 132 KFWASLADIHVNDAFGTAHRAHASNVGIAQFIP-SVAGFLMEKEIKFLSKVTYNPEKPYV 190
           +  A+L D+ V+DAFGTAHRA A+  GIAQF P + AG L+  EI  ++     PE+P V
Sbjct: 132 RKLAALCDVFVHDAFGTAHRAEATTHGIAQFAPIACAGPLLAAEIDAINSALAQPERPLV 191

Query: 191 VVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSRVEEDKIDLAKELL 250
            ++GG+KVS K+ ++ +L  K D++++GG +  TF+ A G  +G S  E   ++ A+ ++
Sbjct: 192 AIVGGSKVSSKLTILQSLASKVDQLIVGGGIANTFMLAAGLNIGKSLAEPGLVEEARAVI 251

Query: 251 EKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIGPETIELFKQKLSD 310
           E  K +G E+ +P D V A+         V +  D + +  + LDIGP+T      +L  
Sbjct: 252 EAMKARGAEVPIPTDVVCAKSFAADAVATVKQAGD-VEDDDLILDIGPDTAARLAAQLKS 310

Query: 311 AKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGAITVVGGGDSAAAVNKFGLEDKFS 370
           A T+VWNGP+GVFE + F++GT+ +A AIA   E  A ++ GGGD+ AA+ ++G+E    
Sbjct: 311 AGTIVWNGPVGVFEFEAFSKGTEGIARAIA---ESSAFSIAGGGDTLAAIAQYGIEKDVG 367

Query: 371 HVSTGGGASLEFLEGKELP 389
           ++STGGGA LE LEGK LP
Sbjct: 368 YISTGGGAFLEVLEGKTLP 386


Lambda     K      H
   0.317    0.137    0.386 

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: 563
Number of extensions: 30
Number of successful extensions: 7
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: 654
Length of database: 400
Length adjustment: 34
Effective length of query: 620
Effective length of database: 366
Effective search space:   226920
Effective search space used:   226920
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: 52 (24.6 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