GapMind for catabolism of small carbon sources

 

Alignments for a candidate for garD in Dyella japonica UNC79MFTsu3.2

Align L-talarate dehydratase (EC 4.2.1.156); galactarate dehydratase (EC 4.2.1.42) (characterized)
to candidate N515DRAFT_1251 N515DRAFT_1251 L-fuconate dehydratase

Query= BRENDA::Q8ZL58
         (398 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1251
          Length = 442

 Score =  121 bits (304), Expect = 3e-32
 Identities = 93/307 (30%), Positives = 145/307 (47%), Gaps = 57/307 (18%)

Query: 113 TKLLWAGASVGRSGMAVQAISPIDIALWDMKAKRAGLPL--------------------- 151
           ++L W G   G   MA+ A+     A WD+ A+RAG PL                     
Sbjct: 101 SQLRWLGPEKGVMHMAIGAVIN---AGWDLAARRAGKPLWRYIAELTPEQLVATIDFRYL 157

Query: 152 ---------------------AKLLGAHRDSVQCYNTSGGFLHTPLDQVLKNVVISRENG 190
                                A++     +    Y TS G+L    +++L+    +  +G
Sbjct: 158 SDAITPDEALQMLRAAEPAKSARIEQLLAEGYPAYTTSPGWLGYTDEKMLRLAREAVADG 217

Query: 191 IGGIKLKVGQPNCAEDIRRLTAVREALGDEFPLMVDANQQWDRETAIRMGRKMEQFNLIW 250
              IKLKVG  +  +D+RR + VR+ +G +  + VDANQ+WD   AI   R++E F+L W
Sbjct: 218 FRTIKLKVGL-SVEDDVRRCSLVRQTVGPDVAIAVDANQRWDVHAAIDWLRRLEGFDLAW 276

Query: 251 IEEPLDAYDIEGHAQLAAALDTPIATGEMLTSFREHEQLILGNASDFVQPDAPRVGGISP 310
           IEEP    D+ GHA +  A+  P++TGE   +    +QL    A D VQ DA RVGG++ 
Sbjct: 277 IEEPTSPDDVLGHAAIRRAVSVPVSTGEHTQNRVIFKQLFQAGAVDLVQIDAARVGGVNE 336

Query: 311 FLKIMDLAAKHGRKLAPHFA----MEVHLHLSAAYPL-------EPWLEHFEWLNPLFNE 359
            L I+ +AAK G ++ PH       E+  HL+ A  +       +  +E  + L+  F++
Sbjct: 337 NLAILLMAAKFGVRVFPHAGGVGLCELVQHLAMADFVAITGRKDDRAIEFVDHLHEHFDD 396

Query: 360 QLELRDG 366
            + +RDG
Sbjct: 397 PVTIRDG 403


Lambda     K      H
   0.319    0.136    0.410 

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: 467
Number of extensions: 23
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 398
Length of database: 442
Length adjustment: 32
Effective length of query: 366
Effective length of database: 410
Effective search space:   150060
Effective search space used:   150060
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