GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tpi in Cupriavidus basilensis 4G11

Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate RR42_RS03200 RR42_RS03200 phosphoglycerate kinase

Query= BRENDA::P36204
         (654 letters)



>FitnessBrowser__Cup4G11:RR42_RS03200
          Length = 402

 Score =  315 bits (806), Expect = 3e-90
 Identities = 177/382 (46%), Positives = 245/382 (64%), Gaps = 9/382 (2%)

Query: 11  LKGKRVIMRVDFNVPVKD-GVVQDDTRIRAALPTIKYALEQGAKVILLSHLGRP-KGEPS 68
           + GKRV +R D NVP  D G + +DTRIRA++P I+  L+ GA V++ SHLGRP +GE  
Sbjct: 16  IAGKRVFIRADLNVPQDDAGQITEDTRIRASVPAIEACLQAGAAVMVTSHLGRPTEGEFK 75

Query: 69  PEFSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRFHPGETKNDP 128
           PE SLAPVA RL+ELLGK VK V   V    +  V  +K GEV+LLEN R + GE KN  
Sbjct: 76  PEDSLAPVAARLAELLGKPVKLVQNWVDGNGE--VSAVKPGEVVLLENCRVNKGEKKNSD 133

Query: 129 ELAKFWASLADIHVNDAFGTAHRAHASNVGIAQFIP-SVAGFLMEKEIKFLSKVTYNPEK 187
           ELA+  A L D++VNDAFGTAHRA A+  GIA++ P + AG L+  EI  L K    P +
Sbjct: 134 ELAQKMAKLCDVYVNDAFGTAHRAEATTHGIAKYAPIACAGPLLAAEIDALGKALGQPAR 193

Query: 188 PYVVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSRVEEDKIDLAK 247
           P V ++ G+KVS K+ ++  L  K D +++GG +  TF+ A G ++G S  E D +  A+
Sbjct: 194 PLVAIVAGSKVSTKLTILKTLAGKVDNLIVGGGIANTFMLAAGLKIGKSLAEADLVADAR 253

Query: 248 ELLEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIGPETIELFKQK 307
            +++    +G  + +PVD V A++        V    D + +  M LDIGP+T ++   +
Sbjct: 254 TIIDLMAARGASVPIPVDVVCAKEFSATAVATVKDAKD-VADDDMILDIGPKTAQMLADQ 312

Query: 308 LSDAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGAITVVGGGDSAAAVNKFGLED 367
           L  A T+VWNGP+GVFE D F+ GTK +A AIA   E  A ++ GGGD+ AA+ K+G+ D
Sbjct: 313 LKLAGTIVWNGPVGVFEFDQFSNGTKVLAQAIA---ESKAFSIAGGGDTLAAIAKYGIAD 369

Query: 368 KFSHVSTGGGASLEFLEGKELP 389
           +  ++STGGGA LEFLEGK+LP
Sbjct: 370 QVGYISTGGGAFLEFLEGKKLP 391


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: 595
Number of extensions: 41
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: 402
Length adjustment: 35
Effective length of query: 619
Effective length of database: 367
Effective search space:   227173
Effective search space used:   227173
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 17 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