GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iolM in Pseudomonas stutzeri RCH2

Align scyllo-inosose 3-dehydrogenase; 2-keto-myo-inositol dehydrogenase; EC 1.1.1.- (characterized)
to candidate GFF1391 Psest_1428 Threonine dehydrogenase and related Zn-dependent dehydrogenases

Query= SwissProt::Q9WYP3
         (395 letters)



>FitnessBrowser__psRCH2:GFF1391
          Length = 362

 Score =  142 bits (359), Expect = 1e-38
 Identities = 118/361 (32%), Positives = 173/361 (47%), Gaps = 48/361 (13%)

Query: 29  WLGSKVWRYPEVRVEEVPEPRIEKPTEIIIKVKACGICGSDVHMAQTDEEGYILYPGLTG 88
           W G K     ++R+E+VP P   +P  + I+V  CGICGSD+H       G +  P    
Sbjct: 12  WHGRK-----DIRLEQVPLPGAPQPGWVQIRVHWCGICGSDLHEYLA---GPVFIPVDAP 63

Query: 89  FPVT-------LGHEFSGVVVEAGPEAINRRTNKRFEIGEPVCAEEMLWCGHCRPCAEGF 141
            P+T       LGHEF G +V  G         + +  G+ V A+    CG CR C  G 
Sbjct: 64  HPLTGIKGQCILGHEFCGEIVAIGEGV------EGYAPGDKVAADACQHCGQCRFCKTGQ 117

Query: 142 PNHCENLNELGFNVDGAFAEYVKVDAKYAWSLRE---LEGVYEGDRLFLAGSLVEPTSVA 198
            N CE L   G   +GAFAE+V V A+  + L E   LE          AG+L+EP +V 
Sbjct: 118 YNLCEQLAFTGLMNNGAFAEFVNVPAELLYRLPEGFPLE----------AGALIEPLAVG 167

Query: 199 YNAVIVRGGGIRPGDNVVILGGGPIGLAAVAILKHAGASKVILSEPSEVRRNLAKELGAD 258
            +AV  +  G   G+ VV++G G IGL  +   K AGA +VI  E S  R+  A E+GA+
Sbjct: 168 MHAV--KKAGSLLGETVVVVGAGTIGLCTIMCAKAAGAGQVIALEMSAARKAKALEVGAN 225

Query: 259 HVIDPTKENFVEAVLDYTNGLGAKLFLEATGVPQLVWPQIEEVIWRARGINATVAIVARA 318
            VIDP++ + +  +   T G GA +  E  G        I+ +  R  G    V I    
Sbjct: 226 WVIDPSECDAIAEIKALTGGYGAGVSFECIGHKATAKLAIDVI--RKAGRCVMVGIFEE- 282

Query: 319 DAKIPLTGEVFQV--RRAQIVGSQGHSGHGTFPRVISLMASG-MDMTKIISKTVSMEEIP 375
               P     F++     Q++GS  ++G   F  VI+L+  G +D+T +I+  + ++ I 
Sbjct: 283 ----PSEFNFFEIVATEKQVIGSLAYAGE--FADVIALIDDGRIDVTPLITGRIGLDNIL 336

Query: 376 E 376
           E
Sbjct: 337 E 337


Lambda     K      H
   0.319    0.138    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: 397
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: 395
Length of database: 362
Length adjustment: 30
Effective length of query: 365
Effective length of database: 332
Effective search space:   121180
Effective search space used:   121180
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: 50 (23.9 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