GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lat in Desulfovibrio vulgaris Miyazaki F

Align Ornithine aminotransferase; Orn-AT; Lysine aminotransferase; Lys-AT; EC 2.6.1.13; EC 2.6.1.36 (characterized)
to candidate 8501786 DvMF_2502 glutamate-1-semialdehyde aminotransferase (RefSeq)

Query= SwissProt::Q5JEW1
         (445 letters)



>FitnessBrowser__Miya:8501786
          Length = 425

 Score =  130 bits (326), Expect = 1e-34
 Identities = 103/338 (30%), Positives = 153/338 (45%), Gaps = 34/338 (10%)

Query: 14  KAKEVIERNFKYLAMTTQDP-------ENLPIVIERGEGIRVYDVDGNVFYDFASGVGVI 66
           ++KE+ ER  + +      P       ++ P+ +   +G  +  VDG  F D+    G +
Sbjct: 4   RSKELFERAQQLIPGGVNSPVRACLGVDSDPLFVAHAKGSHLTTVDGTSFVDYVQSWGPM 63

Query: 67  NVGHSHPRVVEAIKKQAEKFTHYSLTDFFYENAIILAEKLIELAPGDIERKVVYGNSGAE 126
            +GH+HP V  AI    ++ T Y       E+ ++LAE +I+  PG    ++V  NSG E
Sbjct: 64  LLGHAHPVVASAIHAAVDRGTSYGAP---CEDEVVLAEAVIDALPGVEMVRMV--NSGTE 118

Query: 127 ANEAAMKLVKYGTGRKQFLAFYHAFHGRTQAVLSLTASKWVQQDGFFPTMPGVTHIPYPN 186
           A  +A++L +  TGR + + F   +HG   A L+   S             GV  +  P 
Sbjct: 119 ATMSALRLARGVTGRNKVVKFVGCYHGHADAFLASAGS-------------GVATLSIPG 165

Query: 187 PYRNTWGIDGYEEPDELTNRVLDFIEEYVFRHVPPHEIGAIFFEPIQGEGGYVVPPKGFF 246
               T G+      D L     D         +   +I AI  EP+ G  G V+P  GF 
Sbjct: 166 ----TPGVPEATVRDTLLAPYNDLTAVAELFTLHGKDIAAIIVEPVAGNMGLVLPMNGFL 221

Query: 247 KALKKFADEYGILLADDEVQMGIGRTGKFWAIEHFGVEPDLIQFGKAIGGGLPLAGVIHR 306
           + L+    E+G LL  DEV  G  R     A + F + PDL   GK IGGGLP+     R
Sbjct: 222 QGLRDLCTEHGALLIFDEVITGF-RVNYGGAQKRFDITPDLTTLGKIIGGGLPVGAYGGR 280

Query: 307 ADI--TFDKPGR--HATTFGGNPVAIAAGIEVVEIVKE 340
           AD+       G    A T  GNP+A+AAGI  +  +K+
Sbjct: 281 ADLMRRIAPCGEVYQAGTLSGNPLAMAAGIATLAELKK 318


Lambda     K      H
   0.320    0.141    0.418 

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: 430
Number of extensions: 24
Number of successful extensions: 6
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: 445
Length of database: 425
Length adjustment: 32
Effective length of query: 413
Effective length of database: 393
Effective search space:   162309
Effective search space used:   162309
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 51 (24.3 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