GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Shewanella loihica PV-4

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate 5208462 Shew_0974 spermidine/putrescine ABC transporter ATPase subunit (RefSeq)

Query= TCDB::P31134
         (377 letters)



>FitnessBrowser__PV4:5208462
          Length = 378

 Score =  439 bits (1128), Expect = e-128
 Identities = 235/370 (63%), Positives = 278/370 (75%), Gaps = 4/370 (1%)

Query: 7   RPQAKTRKALTPLLEIRNLTKSYDGQHAVDDVSLTIYKGEIFALLGASGCGKSTLLRMLA 66
           +P  KT+  +  LL+I  ++K +D   AVDDVSL I +GEIFALLG SG GKSTLLRMLA
Sbjct: 10  KPTTKTQGEV--LLKIERVSKLFDDVRAVDDVSLNINRGEIFALLGGSGSGKSTLLRMLA 67

Query: 67  GFEQPSAGQIMLDGVDLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEI 126
           GFE+P+ G+I LDG D++ +PPY RPINMMFQSYALFPHMTV QNIAFGLKQDK+PKAEI
Sbjct: 68  GFEKPTEGRIYLDGQDITDMPPYERPINMMFQSYALFPHMTVAQNIAFGLKQDKMPKAEI 127

Query: 127 ASRVNEMLGLVHMQEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRD 186
             RV EML LVHM+ +AKRKP+QLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLR 
Sbjct: 128 EQRVKEMLKLVHMEPYAKRKPNQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRT 187

Query: 187 RMQLEVVDILERVGVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYS 246
           +MQLEVVDILE VGVTCVMVTHDQEEAMTMA RIAIMN G   Q G P +IYE P  R  
Sbjct: 188 QMQLEVVDILEAVGVTCVMVTHDQEEAMTMAERIAIMNDGWIAQTGSPMDIYESPANRMV 247

Query: 247 AEFIGSVNVFEGVLKERQEDGLVLDSPGLVHPLKVDADASV-VDNVPVHVALRPEKIMLC 305
           AEFIGSVN+FEG + E + D +V++   +  P  V    S  VD   V VA+RPEK  + 
Sbjct: 248 AEFIGSVNLFEGDIVEDEVDHVVINVANIPQPFYVGYGVSTSVDTTQVWVAIRPEKTHIS 307

Query: 306 EEPPANGCNFAVGEVIHIAYLGDLSVYHVRLKSGQMISAQLQNAHRHRKGLPTWGDEVRL 365
            E P +  N+  G+V  IAYLG +SVY++RL +GQ+I + + N+ R R   PTW ++V +
Sbjct: 308 REQPEDARNWCAGKVEDIAYLGGISVYYIRLCNGQLIQSVMTNSDR-RADSPTWEEDVFV 366

Query: 366 CWEVDSCVVL 375
            WE  S VVL
Sbjct: 367 SWEATSAVVL 376


Lambda     K      H
   0.321    0.137    0.400 

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: 433
Number of extensions: 12
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: 377
Length of database: 378
Length adjustment: 30
Effective length of query: 347
Effective length of database: 348
Effective search space:   120756
Effective search space used:   120756
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 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