GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tpi in Pandoraea thiooxydans ATSB16

Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate WP_047216139.1 PATSB16_RS01555 phosphoglycerate kinase

Query= BRENDA::P36204
         (654 letters)



>NCBI__GCF_001931675.1:WP_047216139.1
          Length = 397

 Score =  314 bits (804), Expect = 5e-90
 Identities = 171/382 (44%), Positives = 247/382 (64%), Gaps = 12/382 (3%)

Query: 13  GKRVIMRVDFNVPVKD-GVVQDDTRIRAALPTIKYALEQGAKVILLSHLGRP-KGEPSPE 70
           G+RV +R D NVP  D G + +DTRIRA++P I+   + GA V++ SHLGRP +GE  PE
Sbjct: 18  GQRVFIRADLNVPQDDHGNITEDTRIRASVPAIEMCRKAGAAVMVSSHLGRPTEGEFKPE 77

Query: 71  FSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRFHPGETKNDPEL 130
            SLAPVA RLSELLG EVK +   V         ++  G+V+LLEN R + GE KN+ EL
Sbjct: 78  DSLAPVAARLSELLGCEVKLISQWVDGGF-----DVTAGQVVLLENCRLNKGEKKNNDEL 132

Query: 131 AKFWASLADIHVNDAFGTAHRAHASNVGIAQFIP-SVAGFLMEKEIKFLSKVTYNPEKPY 189
           A+  A L DI+VNDAFGTAHRA A+  GIAQ+ P + AG L+  E+  L K    P +P 
Sbjct: 133 ARKMAKLCDIYVNDAFGTAHRAEATTYGIAQYAPVACAGPLLAAELDALGKALGQPARPL 192

Query: 190 VVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSRVEEDKIDLAKEL 249
           V ++ G+KVS K+ ++ +L +K D++++GG +  TF+ A G  +G S  E D ++ AK +
Sbjct: 193 VAIVAGSKVSTKLTILQSLADKVDQLIVGGGIANTFMLAAGLPIGKSLAEADLVEQAKSI 252

Query: 250 LEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIGPETIELFKQKLS 309
           ++   ++G  + +PVD V A++        V    D  P+  M LDIGP++ +   ++L+
Sbjct: 253 IDTMAKRGASVPIPVDVVCAKEFSADASATVKDARDVAPDD-MILDIGPKSAQALAEQLA 311

Query: 310 DAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGAITVVGGGDSAAAVNKFGLEDKF 369
            A T+VWNGP+GVFE D F  GT+ +A AIAA     A ++ GGGD+ AA+ K+G+ ++ 
Sbjct: 312 KAGTIVWNGPVGVFEFDQFGHGTETLARAIAA---SSAFSIAGGGDTLAAIAKYGIANQI 368

Query: 370 SHVSTGGGASLEFLEGKELPGI 391
            ++STGGGA LEFLEG++LP +
Sbjct: 369 DYISTGGGAFLEFLEGRKLPAV 390


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: 557
Number of extensions: 29
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 Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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