GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Dechlorosoma suillum PS

Align Monocarboxylate 2-oxoacid-binding periplasmic protein all3028; Extracellular solute-binding protein; Extracytoplasmic solute receptor protein all3028; TRAP transporter monocarboxylate 2-oxoacid-binding subunit P (characterized)
to candidate Dsui_2650 Dsui_2650 TRAP-type mannitol/chloroaromatic compound transport system, periplasmic component

Query= SwissProt::Q8YSQ6
         (364 letters)



>FitnessBrowser__PS:Dsui_2650
          Length = 330

 Score =  361 bits (927), Expect = e-104
 Identities = 175/323 (54%), Positives = 229/323 (70%), Gaps = 8/323 (2%)

Query: 1   MKRREVLNTAAIATATTALVSCTQTNTSSVQAGLPNVRWRMTTSWPKSLGTFIGA-ETVA 59
           M+RR+ L  A  + A  A        T+    G P VRWR+ +S+PKSL T  GA E +A
Sbjct: 1   MQRRDFLLGAGASAALGAA-------TARAADGQPVVRWRLASSYPKSLDTLYGASEVLA 53

Query: 60  KRVAEMTNGRFKITPFAAGELVPGLQVLDAVQAGTVECGHTSSYYYIGKSPALAFATSVP 119
            RVA +T GRF+I PFAAGE+VPGLQ LDAVQ  TVECGHT   +Y+GK+ A AF + +P
Sbjct: 54  NRVAALTEGRFQIRPFAAGEIVPGLQALDAVQQDTVECGHTLGSFYVGKNRAFAFDSVLP 113

Query: 120 FGLNAQQQYAWLYQGGGLAAIQKIYANFNVINFPAGSTGAQMGGWFKKEIKSVSDLKGLK 179
           FGL  +QQ AW++ G GL  ++++Y ++ VINFP G+TGAQMGGWF+KE++ ++DLKGLK
Sbjct: 114 FGLTTRQQTAWMHFGNGLTLLRELYRDYGVINFPGGNTGAQMGGWFRKELQGLADLKGLK 173

Query: 180 MRIPGLGGQVMSRLGVNVQVLPGGEIYLALDRGAIDAAEWVGPYDDEKLGLNKAAQFYYY 239
           MRIPGLGG++M+RLG   Q +PG ++Y AL++GAIDAAEW GPYDDEKLG  K A++YY+
Sbjct: 174 MRIPGLGGEIMARLGAVPQTIPGADVYPALEKGAIDAAEWSGPYDDEKLGFFKVARYYYH 233

Query: 240 PGWWEPGPTLDVLVNLNAWNRLPKEYQEIFKTATVEANLTMLNQYDALNGEALTRLLAGG 299
           PGWWEP   L  LVN   W +LPK YQ+ F+ A  EA+L    +YDA N  ALTRLLA G
Sbjct: 234 PGWWEPSAQLSFLVNAREWEKLPKAYQQAFEVAAAEAHLLTTAEYDAKNPPALTRLLAQG 293

Query: 300 TKLVPYSQEIMQAAQKISFDIFE 322
            KL  +  ++M+AA + +F  +E
Sbjct: 294 VKLRRFPDDVMKAAYRAAFAFYE 316


Lambda     K      H
   0.317    0.132    0.397 

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: 413
Number of extensions: 15
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: 364
Length of database: 330
Length adjustment: 29
Effective length of query: 335
Effective length of database: 301
Effective search space:   100835
Effective search space used:   100835
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: 49 (23.5 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