GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Marinobacter adhaerens HP15

Align Extracellular solute-binding protein, family 7 (characterized, see rationale)
to candidate GFF4121 HP15_4061 TRAP-type mannitol/chloroaromatic compound transport system, periplasmic component

Query= uniprot:Q48AL6
         (362 letters)



>FitnessBrowser__Marino:GFF4121
          Length = 361

 Score =  448 bits (1153), Expect = e-131
 Identities = 205/352 (58%), Positives = 273/352 (77%), Gaps = 2/352 (0%)

Query: 7   VKAALVVSLGLSSLGLSALAHADDDKKYRWKLAETWGPNFPIFGDATKNMAKMVKEMSNG 66
           ++  L+ ++  ++   S  + A+++  Y  +LA+TWGPN P+ G+  ++MA M + MS+G
Sbjct: 8   IRKTLLAAMAAAATVFSVSSVAEEN--YTLRLAQTWGPNSPVLGETVQHMADMAETMSDG 65

Query: 67  RLTIRIDSSNKHKSALGIFDFVKSGQYQMGHSASYYWKGKNFNTMFFTTVPFGMIASEQH 126
           RL IRID SNKHK+  GIFD V++GQY MGH+ASYY+KG   N M+FTT+PFG+IA E +
Sbjct: 66  RLQIRIDPSNKHKAPFGIFDLVRNGQYDMGHTASYYYKGSIPNAMYFTTIPFGLIAPEMY 125

Query: 127 AWFYYGGGMELMKKVYDQYGIMSFPGGNTGNQMGGWFKKEINSVEDLKGLKMRIPGFAGE 186
           AWFY+G GMELM+KVY+ YG++SFPGGNTGNQMGGWF+KEINS+EDLKGLKMR PGFAGE
Sbjct: 126 AWFYHGEGMELMQKVYEPYGMLSFPGGNTGNQMGGWFRKEINSLEDLKGLKMRTPGFAGE 185

Query: 187 VLAKLGAKPTNIPSGELYTALERNTIDALEWVGPSLDLRMGFHKIAPYYYTGWHEPGTEL 246
           V+++LG   TN+P GELYTALER T+DA+EWVGP+LD +MGFH+IA YYY+GW EPG E+
Sbjct: 186 VMSELGVAVTNLPPGELYTALERGTVDAVEWVGPALDFQMGFHQIAKYYYSGWQEPGAEV 245

Query: 247 QFMVNQKAYNSLPKDLQKILTVAMKAAAYDMYSQSMHASGVNLASLKKDYPNVQMRSFPK 306
           QF++N+K +  LPKDLQ+IL V+M+ AAYDMY QS H SGV    +K+DYP+V  + FP 
Sbjct: 246 QFLINKKTWEELPKDLQEILRVSMRTAAYDMYIQSTHQSGVAWDRMKEDYPDVTHKVFPP 305

Query: 307 PVMEAIVQANDELLEEFAAKDPMTAEILKSLNDYKHQIRAWTNLSDRAYLDN 358
            V++A+    + LL E A KDP+  EI+ S  DY  Q+R WTN+SD+AYL++
Sbjct: 306 EVIDALRSTTNRLLAEAAEKDPLAKEIIDSQRDYLKQVRQWTNISDKAYLNS 357


Lambda     K      H
   0.318    0.133    0.402 

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: 469
Number of extensions: 17
Number of successful extensions: 1
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: 362
Length of database: 361
Length adjustment: 29
Effective length of query: 333
Effective length of database: 332
Effective search space:   110556
Effective search space used:   110556
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