GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt2d in Shewanella oneidensis MR-1

Align mannitol 2-dehydrogenase (NADP+) (EC 1.1.1.138) (characterized)
to candidate 203742 SO4673 threonine 3-dehydrogenase (NCBI ptt file)

Query= BRENDA::Q1ACW3
         (345 letters)



>FitnessBrowser__MR1:203742
          Length = 341

 Score =  157 bits (397), Expect = 4e-43
 Identities = 108/350 (30%), Positives = 180/350 (51%), Gaps = 20/350 (5%)

Query: 7   MKALRYDKPESYA-VVEVPLPTLRDNDVLIKVKACGVCGTDLHIHEGEFIAK----FPLI 61
           MKAL   K E    +V+ P P +  ND+LIK+K   +CGTD+HI+  +  ++     P++
Sbjct: 1   MKALSKLKAEKGIWLVDAPKPEMGHNDLLIKIKKTAICGTDMHIYNWDEWSQKTIPVPMV 60

Query: 62  PGHETVGVVAAIGKDVKGFTVGERVCADNSELCNECFYCRRGQLLLCEKFEAHGVTMDGG 121
            GHE VG V  IG++V+GF +G+RV  +    C  C  CR G+  LC      GV  +G 
Sbjct: 61  VGHEYVGEVVDIGQEVRGFNIGDRVSGEGHITCGHCRNCRAGRTHLCRNTSGVGVNREGS 120

Query: 122 FAEYCAYPAGKVFKI-HNLSDVDATLLEPASCAAHGLEKIAPKIGSSVLMFGAGPTGLCL 180
           FAEY   PA   FKI  ++SD  A++ +P   A H        +G  VL+ GAGP G+  
Sbjct: 121 FAEYLVIPAFNAFKIPDDISDDLASIFDPFGNAVHTALSF-DLVGEDVLITGAGPIGIMA 179

Query: 181 AQL-PHNGASHVVIAAPEGLKMDLAKKLDCADIYVPLSRSNPQAQFDQIKSDNPYGFDIV 239
           A +  H GA HVVI      +++LA+K+  A   V +++ N +    ++      GFD+ 
Sbjct: 180 AAVCRHVGARHVVITDVNEYRLELARKMG-ATRAVNVAQENLKDVMKELGMTE--GFDVG 236

Query: 240 VEATGSPKILEDAINYVRRGGKLVVYGVYSDAARVSWPPSKIFGDEITIIGSFS----ET 295
           +E +G P      ++ +  GGK+ + G+      + W  SK+    + I G +     ET
Sbjct: 237 LEMSGVPSAFRAMLDTMNHGGKIAMLGIPGGEMAIDW--SKVIFKGLVIKGIYGREMFET 294

Query: 296 YMFPATIGYLDTGKVKVEGIVNKTYKLEQWGECLEAMRNKSAIKAAIVFE 345
           +   A++  + +G + +  I+   YK++ + +  +AM +  + K  + ++
Sbjct: 295 WYKMASL--IQSG-LDISPIITHHYKIDDFQKGFDAMGSGQSGKVILSWD 341


Lambda     K      H
   0.320    0.138    0.420 

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: 310
Number of extensions: 18
Number of successful extensions: 5
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: 345
Length of database: 341
Length adjustment: 29
Effective length of query: 316
Effective length of database: 312
Effective search space:    98592
Effective search space used:    98592
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 (21.8 bits)
S2: 49 (23.5 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