GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Sulfuritalea hydrogenivorans DSM 22779

Align C4-dicarboxylate-binding periplasmic protein DctP (characterized)
to candidate WP_041101743.1 SUTH_RS05220 TRAP transporter substrate-binding protein

Query= SwissProt::P37735
         (333 letters)



>NCBI__GCF_000828635.1:WP_041101743.1
          Length = 334

 Score =  416 bits (1068), Expect = e-121
 Identities = 215/331 (64%), Positives = 252/331 (76%), Gaps = 4/331 (1%)

Query: 1   MLTRRILGALVGATALSLALSVPALAEPIVIKFSHVVAPDTPKGKGAAKFEELAEKYTNG 60
           M  R +   LV AT  ++A++      PIVIKFSHVVA DTPKGK +  F + A + T G
Sbjct: 1   MKIRTVFAGLVAATFSAIAMA----QAPIVIKFSHVVAVDTPKGKASEFFAKKAAELTKG 56

Query: 61  AVDVEVYPNSQLYKDKEELEALQLGAVQMLAPSLAKFGPLGVQDFEVFDLPYIFKDYEAL 120
            V VEVY NS LYKDKEE+EALQLGAVQMLAPSLAKFGPLGV++FE FDLPYIF +   L
Sbjct: 57  KVKVEVYANSSLYKDKEEMEALQLGAVQMLAPSLAKFGPLGVKEFEAFDLPYIFDNTAEL 116

Query: 121 HKVTQGEAGKMLLSKLEAKGITGLAFWDNGFKIMSANTPLTMPDDFLGLKMRIQSSKVLE 180
           HK+TQG  G  LL+KLE KGI GLAFWDNGFK  SAN PL  P DF GLKMRIQSSKVLE
Sbjct: 117 HKITQGPVGASLLAKLEPKGIKGLAFWDNGFKSFSANKPLKSPADFKGLKMRIQSSKVLE 176

Query: 181 AEMNALGAVPQVMAFSEVYQALQTGVVDGTENPPSNMFTQKMNEVQKHATVSNHGYLGYA 240
           ++M +LGA+PQVMAFSEVYQALQTGVVDGTENP SN++TQKM+EVQKH T++ HGYLGYA
Sbjct: 177 SQMRSLGALPQVMAFSEVYQALQTGVVDGTENPHSNLYTQKMHEVQKHMTLTEHGYLGYA 236

Query: 241 VIVNKQFWDGLPADVRTGLEKAMAESTDYANGIAKEENEKALQAMKDAGTTEFHELTAEE 300
           VI NK+FWDGLP DVR  LE+AM E+T +AN IAKEEN+ AL+ +K +G T+ +  TA E
Sbjct: 237 VITNKKFWDGLPGDVRGQLEQAMKEATVFANSIAKEENDGALEKIKASGKTQVYSPTAAE 296

Query: 301 RAAWEEVLTPVHDEMAERIGAETIAAVKAAT 331
           R A ++ L   H +M  RIG ETI A+   T
Sbjct: 297 RTAIKKALVKTHTDMESRIGKETIQAIYKET 327


Lambda     K      H
   0.314    0.130    0.364 

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: 350
Number of extensions: 13
Number of successful extensions: 2
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: 333
Length of database: 334
Length adjustment: 28
Effective length of query: 305
Effective length of database: 306
Effective search space:    93330
Effective search space used:    93330
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 49 (23.5 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