GapMind for catabolism of small carbon sources

 

Alignments for a candidate for odc in Phaeobacter inhibens BS107

Align ornithine decarboxylase (EC 4.1.1.17) (characterized)
to candidate GFF1150 PGA1_c11650 putative lysine/ornithine decarboxylase

Query= BRENDA::G4XUJ8
         (413 letters)



>FitnessBrowser__Phaeo:GFF1150
          Length = 383

 Score =  158 bits (400), Expect = 2e-43
 Identities = 119/347 (34%), Positives = 178/347 (51%), Gaps = 26/347 (7%)

Query: 74  YAVKCNPEPALLGSLAAMG-ANFDCASRAEIEAVLSLRVSPDRIV-YANPCKQESHIKYA 131
           YAVK NP PA+L +L A G   FD AS AE++AV +   SPD ++ Y NP + +  I   
Sbjct: 49  YAVKANPHPAVLSNLVAAGITGFDVASPAEMDAVRA--ASPDAVMHYNNPVRSDVEIAAG 106

Query: 132 ASVGVNLTTFDSKDELEKMRKWHPKCALLLRVKAPEDGGARCPLGPKYGALPEEVIPLLQ 191
            + GV   + D   EL+K+      C + +R   P   GA    G K+GA P+  I LL+
Sbjct: 107 IAHGVASWSVDEPSELDKLADVPKSCEIAVRFALPV-AGAAYDFGSKFGAEPDMAIELLK 165

Query: 192 AAQAARLSVVGASFHIGSGATHFSSYRGAIAEAKKVFETAVKMGMPRMTMLNIGGGFTAG 251
              AA        FH G+     S++   +  AK++ + A   G+ ++  LN+GGGF A 
Sbjct: 166 RV-AAEGWTPALCFHPGTQCEDESAWVEYVHAAKRIIDAA---GV-KIARLNVGGGFAAN 220

Query: 252 SQ-----FDEAATAIKSALQTYFPNE-PGLTIISEPGRFFAESAFTLATNVIGRRVRGEL 305
                   ++   AI  A+   F ++ PGL  I EPGR     +FTLA  + G R  GE+
Sbjct: 221 RDGVAPDLEKVFAAIWVAVDAAFGDDKPGL--ICEPGRAMVSESFTLAARIKGIRKAGEV 278

Query: 306 REYWINDGIYGSMNCILYDHATVTCKPLACTSSRANPMCKGARVYNSTVFGPTCDALDTV 365
              ++NDG+YG +  I         + +A   +R     +GA      VFGPTCD+LD +
Sbjct: 279 --VFLNDGVYGGLVDIRDMGLPGRVEVVAADGTR-----RGADAQPRVVFGPTCDSLDRL 331

Query: 366 MTGHLLP-DLQVSDWLVFPNMGAYTAAAGSSFNGFKTAAILTYLAYS 411
             G  LP D Q+ D+++FP +GAY++A  + FNG+  + + T +  S
Sbjct: 332 PDGLPLPRDTQIGDYVLFPGLGAYSSAMSTQFNGYGLSDVATVIELS 378


Lambda     K      H
   0.320    0.134    0.406 

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: 427
Number of extensions: 25
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: 413
Length of database: 383
Length adjustment: 31
Effective length of query: 382
Effective length of database: 352
Effective search space:   134464
Effective search space used:   134464
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: 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