GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tpiA in Xenophilus azovorans DSM 13620

Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate WP_038200447.1 Q392_RS01395 phosphoglycerate kinase

Query= BRENDA::P36204
         (654 letters)



>NCBI__GCF_000745855.1:WP_038200447.1
          Length = 397

 Score =  315 bits (806), Expect = 3e-90
 Identities = 180/380 (47%), Positives = 245/380 (64%), Gaps = 13/380 (3%)

Query: 13  GKRVIMRVDFNVPVKD-GVVQDDTRIRAALPTIKYALEQGAKVILLSHLGRPK-GEPSPE 70
           G+RV +R D NVP  D G + +DTRIRA++P I+ AL+ GA V++ SHLGRPK GE  PE
Sbjct: 17  GQRVFIRADLNVPQDDSGAITEDTRIRASVPCIRMALDAGAAVMVTSHLGRPKEGEFKPE 76

Query: 71  FSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRFHPGETKNDPEL 130
            SLAPVA RL ELLG+EV  V   V D V     ++K G V+LLEN R + GE KND  L
Sbjct: 77  DSLAPVAARLGELLGREVPLVADWV-DGV-----DVKPGGVVLLENCRLNKGEKKNDEAL 130

Query: 131 AKFWASLADIHVNDAFGTAHRAHASNVGIAQFIP-SVAGFLMEKEIKFLSKVTYNPEKPY 189
           A+  A+L DI+VNDAFGTAHRA A+  GIAQF   + AG L+  EI  +SK    P++P 
Sbjct: 131 ARKLAALTDIYVNDAFGTAHRAEATTYGIAQFARVACAGPLLAAEIDAISKALAQPKRPL 190

Query: 190 VVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSRVEEDKIDLAKEL 249
           V ++ G+KVS K+ ++ +L +  D++++GG +  TF+ A G  +G S  E D +  AK +
Sbjct: 191 VAIVAGSKVSTKLTILQSLAKNVDQLIVGGGIANTFMLAAGLPIGKSLAEPDLLGEAKAV 250

Query: 250 LEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIGPETIELFKQKLS 309
           +E  + +G  + +PVD V A+         V    D + E  + LDIGP+T E    +L 
Sbjct: 251 IEAMRARGAAVPIPVDVVTAKTFAADAPATVKAAAD-VAEDDLILDIGPKTAEQLAAQLR 309

Query: 310 DAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGAITVVGGGDSAAAVNKFGLEDKF 369
           +A T+VWNGP+GVFE D FA GT+ +A AIAA     A ++ GGGD+ AA+ K+G+E   
Sbjct: 310 EAGTIVWNGPVGVFEFDAFAHGTETIARAIAA---SSAFSIAGGGDTLAAIAKYGIEKDV 366

Query: 370 SHVSTGGGASLEFLEGKELP 389
            ++STGGGA LE LEGK+LP
Sbjct: 367 GYISTGGGAFLEVLEGKQLP 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: 591
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: 397
Length adjustment: 34
Effective length of query: 620
Effective length of database: 363
Effective search space:   225060
Effective search space used:   225060
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 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