GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1750 in Pseudomonas simiae WCS417

Align TM1750, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate GFF1588 PS417_08080 ABC transporter ATP-binding protein

Query= TCDB::Q9X272
         (328 letters)



>FitnessBrowser__WCS417:GFF1588
          Length = 323

 Score =  252 bits (644), Expect = 8e-72
 Identities = 139/300 (46%), Positives = 192/300 (64%), Gaps = 2/300 (0%)

Query: 23  FPQGKRILKAVDGISIEIKEGETLGLVGESGCGKSTLGRTILKLLRPDGGKIFFEGKDIT 82
           F   K+ ++AV+G+S+ +  GETLGLVGESG GKSTLGR IL L     G++ F+G D+ 
Sbjct: 21  FGLNKQWVRAVNGVSLSLAAGETLGLVGESGSGKSTLGRAILHLNPISAGQVLFDGIDMA 80

Query: 83  NLNDKEMKPYRKKMQIIFQDPLGSLNPQMTVGRIIEDPLIIHKIGTKKERRKRVEELLDM 142
           + +  ++   R +  +IFQDP  +LNP+ T+G  I + L + +    +    RV ELLD+
Sbjct: 81  HGSAIDITRLRHETAMIFQDPYAALNPRHTIGETIAEVLRVQRKVAPERISDRVNELLDL 140

Query: 143 VGIGREFINSFPHEFSGGQQQRIGIARALALNPKFIVCDEPVSALDVSIQAQIIDLLEEI 202
           VG+  E  +  P   SGGQ QR+GIARALA+ P+ I+ DE V+ALDVSIQ QII+LL E+
Sbjct: 141 VGLRPELASRKPGSLSGGQCQRVGIARALAVEPRLIIADECVAALDVSIQGQIINLLLEL 200

Query: 203 QQKMGISYLFIAHNLAVVEHISHKVAVMYLGKIVEYGDVDKIFLNPIHPYTRALLKSVPK 262
           QQ+M ++ LFIAH+LA+V  +  +VAVMYLGKIVE G V+ +F  P HPYT AL++++P+
Sbjct: 201 QQRMHLAILFIAHDLAIVRRLCDRVAVMYLGKIVEEGPVESVFTAPRHPYTAALIQAIPE 260

Query: 263 IPWDGQKQRFYSLKGELPSPIDLPKGCRFQTRCTEKKAICFEKEPELTEVEKNHFVSCHL 322
           I    +      L GE PSP++LP GC F  RC   + +C    P  T     H  SC L
Sbjct: 261 ID-PHRPLPTEPLPGEPPSPLNLPTGCAFHPRCRHARTMCSVVLPP-THFLHEHRYSCVL 318


Lambda     K      H
   0.321    0.142    0.417 

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: 322
Number of extensions: 13
Number of successful extensions: 2
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: 328
Length of database: 323
Length adjustment: 28
Effective length of query: 300
Effective length of database: 295
Effective search space:    88500
Effective search space used:    88500
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: 48 (23.1 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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