GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potD in Marinobacter adhaerens HP15

Align spermidine/putrescine ABC transporter, periplasmic spermidine/putrescine-binding protein PotD (characterized)
to candidate GFF4125 HP15_4065 spermidine/putrescine ABC transporter periplasmic substrate-binding protein

Query= CharProtDB::CH_088339
         (348 letters)



>FitnessBrowser__Marino:GFF4125
          Length = 346

 Score =  371 bits (953), Expect = e-107
 Identities = 172/345 (49%), Positives = 248/345 (71%), Gaps = 2/345 (0%)

Query: 6   RHLLAAGALALGMSAAHADDNNTLYFYNWTEYVPPGLLEQFTKETGIKVIYSTYESNETM 65
           + L  AG LA+G++   +++   L  YNW+EY+P  +L++FT+ETGI+V+Y+TY+SNE M
Sbjct: 2   KKLALAGLLAVGLTGCSSEEPQVLNLYNWSEYMPQEVLDRFTEETGIQVVYTTYDSNEAM 61

Query: 66  YAKLKTYKDGA-YDLVVPSTYYVDKMRKEGMIQKIDKSKLTNFSNLDPDMLNKPFDPNND 124
           YA+LK   D A YDL VPSTYYV KMR+E ++  ID+SK+  F NLDP+++N   DP N 
Sbjct: 62  YARLKLLDDSAAYDLAVPSTYYVSKMRQEDLLLPIDRSKIEGFDNLDPELVNLDIDPENQ 121

Query: 125 YSIPYIWGATAIGVNGDAVDPKSVTSWADLWKPEYKGSLLLTDDAREVFQMALRKLGYSG 184
           +S+PY+WG T + V+   ++ + VT+W DLW+  + G ++LT+D REVF + LR LGYSG
Sbjct: 122 FSVPYLWGTTGLAVDTADIEGEPVTAWEDLWEDRFDGRVMLTNDMREVFHVGLRVLGYSG 181

Query: 185 NTTDPKEIEAAYNELKKLMPNVAAFNSDNPANPYMEGEVNLGMIWNGSAFVARQAGTPID 244
           N+T+P EIEAAY +L +LMP+V  FNSD P  PY+EGE ++GMIWNG A + +     ++
Sbjct: 182 NSTNPDEIEAAYEKLAELMPSVRTFNSDAPRMPYLEGEADVGMIWNGEAVMGKDTMESLE 241

Query: 245 VVWPKEGGIFWMDSLAIPANAKNKEGALKLINFLLRPDVAKQVAETIGYPTPNLAARKLL 304
            V+P+EG I W+DS  IP NAKN E A + I+F+L+P+++  ++E IGY TPNLAAR LL
Sbjct: 242 YVYPEEGIIAWLDSFVIPKNAKNPEAAHQFISFVLQPEISALISEEIGYATPNLAARDLL 301

Query: 305 SPEVANDKTLYPDAETIKNGEWQNDVG-AASSIYEEYYQKLKAGR 348
             EVAN++  YP+A  + N E+Q D+G  A  +Y +Y++ LK+GR
Sbjct: 302 PDEVANNRASYPNATDMINAEFQTDIGDDALQVYAKYWEMLKSGR 346


Lambda     K      H
   0.314    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: 461
Number of extensions: 16
Number of successful extensions: 3
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: 348
Length of database: 346
Length adjustment: 29
Effective length of query: 319
Effective length of database: 317
Effective search space:   101123
Effective search space used:   101123
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 (21.9 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