GapMind for catabolism of small carbon sources

 

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

Align Broad specificity amino-acid racemase; Broad spectrum racemase; EC 5.1.1.10 (characterized)
to candidate 203001 SO3916 alanine racemase, biosynthetic (NCBI ptt file)

Query= SwissProt::Q88GJ9
         (409 letters)



>FitnessBrowser__MR1:203001
          Length = 358

 Score =  113 bits (283), Expect = 8e-30
 Identities = 111/364 (30%), Positives = 178/364 (48%), Gaps = 37/364 (10%)

Query: 47  EVSASALQHNIRTLQAELAGKSKLCAVLKADAYGHGIGLVMPSIIAQGVPCVAVASNEEA 106
           E+S+SALQ+N+  L+ + A  S++ AV+KA+ YGHG+  V   +         +A  EEA
Sbjct: 8   EISSSALQNNLAVLRQQ-ASSSQVMAVVKANGYGHGLLNVAKCL--NNADGFGLARLEEA 64

Query: 107 RVVRASGFTGQLVRVR-LASLSELEDGLQYDMEELV---GSAEFARQADAIAARHGKTLR 162
             +RA     +L+ +      ++L   +++D++ +V      E   QA        K + 
Sbjct: 65  LELRAGSVKARLLLLEGFFRSTDLPLLVEHDIDTVVHHESQIEMLEQATL-----SKPVT 119

Query: 163 IHMALNSSGMSRNGVEMATWSGRGEALQITDQKHL-KLVALMTHFAVEDKDD---VRKGL 218
           + + ++S GM R GV    +S      ++T  K++ K + LMTHFA  D+ D    +  +
Sbjct: 120 VWLKVDS-GMHRLGVTPEQFSA--VYARLTACKNVAKPIHLMTHFACADEPDNHYTQVQM 176

Query: 219 AAFNEQTDWLIKHARLDRSKLTLHAANSFATLEVPEARLDMVRTGGALFGDT-----VPA 273
             FN+ T  L     L         ANS   L  P+++ D +R G A++G +       A
Sbjct: 177 QTFNQLTADLPGFRTL---------ANSAGALYWPKSQGDWIRPGIAMYGVSPVTGDCGA 227

Query: 274 RTEYKRAMQFKSHVAAVHSYPAGNTVGYDRTFTLARDSRLANITVGYSDGYRRVFTNKGH 333
                 AM   S + AV  + A   VGY   +T  +D+RL  + +GY DGY R       
Sbjct: 228 NHGLIPAMNLVSRLIAVREHKANQPVGYGCYWTAKQDTRLGVVAIGYGDGYPRNAPEGTP 287

Query: 334 VLINGHRVPVVGKVSMNTLMVDVTDFPDVKGGNEVVLFGKQAGGEITQAEMEEINGALLA 393
           V ING RVP+VG+VSM+ L VD+      + G++V+L+G+    E    E+ E  G +  
Sbjct: 288 VWINGRRVPIVGRVSMDMLTVDLGHDATDQVGDDVLLWGQALPVE----EVAEHIGTIAY 343

Query: 394 DLYT 397
           +L T
Sbjct: 344 ELVT 347


Lambda     K      H
   0.318    0.132    0.377 

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: 293
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: 409
Length of database: 358
Length adjustment: 30
Effective length of query: 379
Effective length of database: 328
Effective search space:   124312
Effective search space used:   124312
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 (21.7 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