GapMind for catabolism of small carbon sources

 

Alignments for a candidate for proV in Herbaspirillum seropedicae SmR1

Align glycine betaine/l-proline transport atp-binding protein prov (characterized)
to candidate HSERO_RS08545 HSERO_RS08545 glycine/betaine ABC transporter ATP-binding protein

Query= CharProtDB::CH_001555
         (400 letters)



>FitnessBrowser__HerbieS:HSERO_RS08545
          Length = 377

 Score =  193 bits (491), Expect = 6e-54
 Identities = 118/358 (32%), Positives = 201/358 (56%), Gaps = 20/358 (5%)

Query: 36  EKTGLSLGVKDA-SLAIEEGEIFVIMGLSGSGKSTMVRLLNRLIEPTRGQVLIDGVDIAK 94
           +K G  +   DA SL + EGEI V +G SG GK+T ++++NRLI PT G+VL++G D + 
Sbjct: 13  QKDGTQVKAVDAVSLKVAEGEICVFLGPSGCGKTTTLKMINRLINPTSGRVLLNGQDTSG 72

Query: 95  ISDAELREVRRKKIAMVFQSFALMPHMTVLDNTAFGMELAGINAEERREKALDALRQVGL 154
           I + ELR    + I  V Q   L P+MT+ +N      L G + +  +E+A + +  V L
Sbjct: 73  IDEVELR----RHIGYVIQQIGLFPNMTIEENITIVPRLLGWDKKRCQERATELMAMVAL 128

Query: 155 E--NYAHSYPDELSGGMRQRVGLARALAINPDILLMDEAFSALDPLIRTEMQDELVKLQA 212
           +   +   YP ELSGG +QR+G+ RALA +  +LLMDE F A+DP+ R  +Q+E  ++Q 
Sbjct: 129 DPKKFLKRYPRELSGGQQQRIGVIRALAADAPVLLMDEPFGAVDPINRESIQNEFFQMQR 188

Query: 213 KHQRTIVFISHDLDEAMRIGDRIAIMQNGEVVQVGTPDEILNNPANDYVRTFFRGVDIS- 271
           +  +T++ +SHD+DEA+++GD++A+ + G++VQ   PD +L  P +D+V  F  G D + 
Sbjct: 189 QLNKTVIMVSHDIDEAIKLGDKVAVFRAGKLVQFDNPDTLLARPKDDFVSAFV-GQDHTL 247

Query: 272 ---QVFSAKDIARRTPNGLIRKTPGFGPRSALKLLQDEDREYGYVIERGNKFVGAVSIDS 328
               +  A + A   P       P      AL L+ D+D  Y  +I+  N+ +G ++   
Sbjct: 248 KRLLLVRAGEAATTPPTA----HPDVSCDQALALMDDQDSRYLTIIDADNRALGYLTRRD 303

Query: 329 LKTAL-TQQQGLDAALIDAPLAVDAQTPLSELLSHVGQAPCAVPVVDEDQQYVGIISK 385
           ++ +    +  +    ++A    + +  LS++  H   +   +PV+  D  YVG +++
Sbjct: 304 VRGSTGVAEDKVRPFTMNADPDENLRVVLSKMYKH---STSWMPVIANDGSYVGEVTQ 358


Lambda     K      H
   0.319    0.137    0.378 

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: 370
Number of extensions: 16
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 400
Length of database: 377
Length adjustment: 30
Effective length of query: 370
Effective length of database: 347
Effective search space:   128390
Effective search space used:   128390
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 (21.7 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