GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1750 in Phyllobacterium brassicacearum STM 196

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 WP_106712846.1 CU102_RS19975 ABC transporter ATP-binding protein

Query= TCDB::Q9X272
         (328 letters)



>NCBI__GCF_003010955.1:WP_106712846.1
          Length = 336

 Score =  282 bits (722), Expect = 7e-81
 Identities = 142/306 (46%), Positives = 200/306 (65%), Gaps = 2/306 (0%)

Query: 17  VDLKKYFPQGKRILKAVDGISIEIKEGETLGLVGESGCGKSTLGRTILKLLRPDGGKIFF 76
           + LK    +   I+ A+DG+ + I++GE +GLVGESGCGKSTLGR I  +  P  G I +
Sbjct: 28  IALKLKLARPASIVHALDGVDLTIQKGEVVGLVGESGCGKSTLGRVIAGITSPSEGSILW 87

Query: 77  EGKDITNLNDKEMKPYRKKMQIIFQDPLGSLNPQMTVGRIIEDPLIIHKIGTKKERRKRV 136
           EG+D   +  ++        Q+IFQ+P+ +LNP+MTV  +I +    H    + ERR  V
Sbjct: 88  EGEDRATMPTEKRHRLGLITQMIFQNPMAALNPRMTVDELIWEAPSTHGFARRSERRDYV 147

Query: 137 EELLDMVGIGREFINSFPHEFSGGQQQRIGIARALALNPKFIVCDEPVSALDVSIQAQII 196
           ++ L + G        +PH+FSGGQ+QR+ IARALA+ PKF+VCDE V+ALDVSIQAQ++
Sbjct: 148 DKYLRLAGFDPAMKTRYPHQFSGGQRQRVNIARALAVQPKFLVCDESVAALDVSIQAQVL 207

Query: 197 DLLEEIQQKMGISYLFIAHNLAVVEHISHKVAVMYLGKIVEYGDVDKIFLNPIHPYTRAL 256
           +L  E++ K+ ++YLF++H+L VVEHIS +VA+MYLG+IVE   V++IF  P HPYT+AL
Sbjct: 208 NLFMELRDKLDLTYLFVSHDLGVVEHISDRVAIMYLGRIVEEAPVEEIFKRPNHPYTQAL 267

Query: 257 LKSVPKIPWDGQKQRFYSLKGELPSPIDLPKGCRFQTRCTEKKAICFEKEPELTEVEKNH 316
           L  VP+I  +  K+RF  +KGELPSP++ P GC F  RC      C    P   E+   H
Sbjct: 268 LAEVPRI--ESGKRRFQVVKGELPSPLNPPTGCHFHPRCPFAMDRCRIDAPVKREIAPGH 325

Query: 317 FVSCHL 322
             +CHL
Sbjct: 326 MSACHL 331


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: 347
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: 336
Length adjustment: 28
Effective length of query: 300
Effective length of database: 308
Effective search space:    92400
Effective search space used:    92400
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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