GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tpi in Rhizobium etli CFN 42

Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate WP_011426722.1 RHE_RS17890 phosphoglycerate kinase

Query= BRENDA::P36204
         (654 letters)



>NCBI__GCF_000092045.1:WP_011426722.1
          Length = 418

 Score =  344 bits (882), Expect = 5e-99
 Identities = 181/384 (47%), Positives = 245/384 (63%), Gaps = 2/384 (0%)

Query: 10  DLKGKRVIMRVDFNVPVKDGVVQDDTRIRAALPTIKYALEQGAKVILLSHLGRPKGEPSP 69
           D+ GKRV++RVD NVPVKDG V D TRI    PTI    ++GAKVILL+H GRPK  PSP
Sbjct: 30  DISGKRVLVRVDLNVPVKDGKVTDTTRIERVAPTILELSDKGAKVILLAHFGRPKDGPSP 89

Query: 70  EFSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRFHPGETKNDPE 129
           + SL+ +A  + E+L   V      +G+    AV  +  G++LLLENTRFH GE KNDP+
Sbjct: 90  DLSLSLIAPSVEEVLDHAVLTASDCIGEAATAAVAGMNNGDILLLENTRFHKGEEKNDPD 149

Query: 130 LAKFWASLADIHVNDAFGTAHRAHASNVGIAQFIPSVAGFLMEKEIKFLSKVTYNPEKPY 189
             K  A+  DI+VNDAF  AHRAHAS  G+A  +P+ AG  M+ E++ L K    P +P 
Sbjct: 150 FTKALAANGDIYVNDAFSAAHRAHASTEGLAHHLPAYAGRTMQAELEALEKGLGAPARPV 209

Query: 190 VVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSRVEEDKIDLAKEL 249
           V ++GGAKVS KI ++ NL++K D ++IGG M  TF+ A G  VG S  E D  + AK++
Sbjct: 210 VAIVGGAKVSTKIDLLMNLVKKVDALVIGGGMANTFIAARGTNVGKSLCEHDLAETAKQI 269

Query: 250 LEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIGPETIELFKQKLS 309
           + +A   G  I+LP D V+A++   G   + V I + IP   M LD+GP+++E     + 
Sbjct: 270 MIEAATSGCAIILPEDGVVAREFRAGAANETVDI-NAIPADAMVLDVGPKSVEAINAWIE 328

Query: 310 DAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGAIT-VVGGGDSAAAVNKFGLEDK 368
            A T+VWNGP+G FEI+ F   T   A   A  T  G +T V GGGD+ +A+N  G+ D 
Sbjct: 329 RAATLVWNGPLGAFEIEPFDTATVAAAKYAAERTAAGKLTSVAGGGDTVSALNHAGVADD 388

Query: 369 FSHVSTGGGASLEFLEGKELPGIA 392
           F++VST GGA LE++EGKELPG+A
Sbjct: 389 FTYVSTAGGAFLEWMEGKELPGVA 412


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: 582
Number of extensions: 27
Number of successful extensions: 3
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: 418
Length adjustment: 35
Effective length of query: 619
Effective length of database: 383
Effective search space:   237077
Effective search space used:   237077
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