GapMind for catabolism of small carbon sources

 

Alignments for a candidate for scrT in Caulobacter crescentus NA1000

Align sucrose permease scrT (characterized)
to candidate CCNA_01191 CCNA_01191 transporter, major facilitator superfamily

Query= reanno::ANA3:7022816
         (406 letters)



>FitnessBrowser__Caulo:CCNA_01191
          Length = 411

 Score =  457 bits (1176), Expect = e-133
 Identities = 230/386 (59%), Positives = 288/386 (74%)

Query: 16  IRVLTYLMFFMFAMTSDAVGVIIPQLISEFGLSLSQASAFHYMPMIFIAISGLFLGFLAD 75
           IR+LTYLMF MFAMT+D+VGVIIP +I  F L ++ A +FHY  M  IA+ G+ LGFLAD
Sbjct: 15  IRILTYLMFMMFAMTTDSVGVIIPHVIKTFDLGMAAAGSFHYASMTGIALGGVCLGFLAD 74

Query: 76  KIGRKLTILLGLLLFAIACFLFALGESFYYFLLLLALVGLAIGVFKTGALALIGDISRST 135
           ++GRK TI+LGL+ FA+  FLFA+G+ F +F+ LL L GLAIGVFKTGALALIGDIS ST
Sbjct: 75  RLGRKATIVLGLVAFAVTAFLFAVGKDFGFFVALLFLSGLAIGVFKTGALALIGDISSST 134

Query: 136 KQHSSTMNTVEGFFGVGAMVGPAIVSYLLISGVSWKYLYFGAGVFCLLLCWLAFRADYPQ 195
           + H++TMN VEGFFG+GA++GPAIV+ LL  G SWK+LY  AG  C+LL   A    YPQ
Sbjct: 135 RAHTATMNMVEGFFGLGAILGPAIVTALLAQGASWKWLYVIAGALCVLLIIAALNVRYPQ 194

Query: 196 VKRSSTETINLTNTFSMMKNPYALGFSLAIGLYVATEVAIYVWMPSLLQEYQGDYTVLAA 255
              ++ + ++   T +M  NPYAL FS AI LYV  E AIYVWMP+LL +Y+G   +LAA
Sbjct: 195 TPPAAQQKLDPRVTLAMFGNPYALAFSFAIMLYVGVETAIYVWMPTLLADYKGPAVLLAA 254

Query: 256 YALTIFFTLRAGGRFLGGWILNHFSWQQVMFWFSLAISLCYLGSMLYGVEAAVILLPLSG 315
           YAL++FF LRA GRFLG W+LN  SW QV+   S+AI +C+  ++  G   AV  LP+SG
Sbjct: 255 YALSVFFILRAAGRFLGAWLLNRLSWTQVVAICSVAILICFAAALAGGRAVAVYSLPISG 314

Query: 316 LFMSMMYPTLNSKGISCFPVAQHGSVAGVILFFTAVSAALAPLCMGLVGDIFGHVKYGFY 375
           LFMS++YPT+NSKGISCFP A+HGSV+GVILFFT VSA +AP  MGL+ D FG   YGF 
Sbjct: 315 LFMSVLYPTINSKGISCFPKAEHGSVSGVILFFTCVSAVIAPWMMGLISDRFGDAVYGFA 374

Query: 376 LATGFAVLLCLLAGVNLIKDPSQALL 401
           LATG A LL +LA +NL+ DPS+A L
Sbjct: 375 LATGLAALLAVLAVLNLVFDPSRARL 400


Lambda     K      H
   0.330    0.143    0.437 

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: 532
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: 406
Length of database: 411
Length adjustment: 31
Effective length of query: 375
Effective length of database: 380
Effective search space:   142500
Effective search space used:   142500
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.9 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