GapMind for catabolism of small carbon sources

 

Alignments for a candidate for garD in Desulfitobacterium hafniense DCB-2

Align Galactarate dehydratase (EC 4.2.1.42) (characterized)
to candidate WP_011460067.1 DHAF_RS16340 UxaA family hydrolase

Query= reanno::WCS417:GFF829
         (517 letters)



>NCBI__GCF_000021925.1:WP_011460067.1
          Length = 385

 Score =  214 bits (544), Expect = 6e-60
 Identities = 145/381 (38%), Positives = 200/381 (52%), Gaps = 26/381 (6%)

Query: 119 GYRNADGTVGTRNILGITTTVQCVTGVLDHAVKRIKDELLPKYPHVDDVVALTHSYGCGV 178
           G+R  DG  G RN L I  T  C T V  +   +           V   VA+ + +GC  
Sbjct: 5   GFRRPDGLFGIRNHLLILPTSVCATTVAANIAAQ-----------VPGAVAIANQHGC-- 51

Query: 179 AITATDAYIPIRTVRNLARNPNLGGEALVISLGCEKLQAGQVMHDNDSSVDLSEPWLYRL 238
                D    +RT+  + RNPN+G   LV+ LGCE +    ++H  +      +P +  L
Sbjct: 52  CQLGADYEQTLRTLIGIGRNPNVGA-VLVVGLGCEGIP---ILHTAEEIAKSGKP-VQSL 106

Query: 239 QDSSHGFTEMIEQI-MALAETRLKKLDQRRRETVPASELILGMQCGGSDAFSGITANPAL 297
               HG T     + + +A    + L   +RE  P SEL LG++CGGSD  SG+ ANPA 
Sbjct: 107 IIQEHGGTLKTTALGVQVAAQMARTLSMLKREEAPLSELSLGVECGGSDFTSGLAANPAA 166

Query: 298 GYASDLLLRAGATVMFSEVTEVRDAIYLLTSRAENTQVAQEL---VREMDWYDRYLAKGE 354
           G ASDL+++AG T M SE TE   A ++L  RA++ +VA +L   V+E +   R L    
Sbjct: 167 GTASDLVVKAGGTAMLSETTEFIGAEHVLAKRAKSPEVAAKLLGIVKETELRARQL---H 223

Query: 355 AD-RSANTTPGNKKGGLSNIVEKSLGSIVKSGSSAINGVLGPGERFKGKGLIFCATPASD 413
            D R    TPGN  GG+S+I EKSLG I K+G S I  +L  GE  +GKGL    TP  D
Sbjct: 224 VDLRDGQPTPGNIAGGISSIEEKSLGCIYKAGHSTIQDILAYGEAPQGKGLYVMDTPGQD 283

Query: 414 FVCGTLQLAAGMNLHVFTTGRGTPYGLAMAPVVKVSTRTELAQRWPDLIDIDAGRIATGR 473
                  LA G+ + VFTTGRGTP G  +APV+KV+   +      D ID+D   I +G 
Sbjct: 284 VESMIGMLAGGIQIIVFTTGRGTPTGSPIAPVIKVTANADTYLNMADNIDLDLSPILSGA 343

Query: 474 ATIEELGWELFHFYLDVASGR 494
            TIE+ G  +F   ++VA+G+
Sbjct: 344 ETIEDSGRRIFKEIIEVANGK 364


Lambda     K      H
   0.318    0.135    0.401 

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: 492
Number of extensions: 22
Number of successful extensions: 4
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: 517
Length of database: 385
Length adjustment: 32
Effective length of query: 485
Effective length of database: 353
Effective search space:   171205
Effective search space used:   171205
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: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. 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