GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1749 in Paraburkholderia bryophila 376MFSha3.1

Align TM1749, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate H281DRAFT_03126 H281DRAFT_03126 oligopeptide transport system ATP-binding protein

Query= TCDB::Q9X271
         (324 letters)



>FitnessBrowser__Burk376:H281DRAFT_03126
          Length = 333

 Score =  302 bits (774), Expect = 7e-87
 Identities = 164/327 (50%), Positives = 214/327 (65%), Gaps = 7/327 (2%)

Query: 2   MELLNVNNLKVEFHRVEGI-VKAVDGISYKLNKGESLGIVGESGSGKSVSVLSLLRLINR 60
           M LL V +L V F R EG  V AV  +S+ L  G +LGIVGESGSGKS +V++LL L+  
Sbjct: 1   MPLLEVKDLSVRFTRREGAPVDAVQRVSFSLEPGRTLGIVGESGSGKSQTVMALLGLLAG 60

Query: 61  NGRIVDGEAIFLGKDLLKLNKEELRNIRGKDISIIFQNPMTSLNPIIRVGIQVMEPIIWH 120
           NG  V GEA++ G++LL +N+  L  IRG  I +IFQ+PMTSLNP + +  Q+ E +  H
Sbjct: 61  NGN-VSGEALYRGENLLAMNEAALNKIRGDRIGMIFQDPMTSLNPFLTIERQMTETLQLH 119

Query: 121 RLMKNEEARERAIELLERVGIPESPKRFLNYPFQFSGGMRQRVMIAMALACHPKLLIADE 180
           R M   +AR RAIE LE V IP+S +R   YP +FSGGMRQRVMIAMAL   P++LIADE
Sbjct: 120 RKMSRRDARRRAIETLETVRIPDSARRIGMYPHEFSGGMRQRVMIAMALLSEPEILIADE 179

Query: 181 PTTALDVTIQAQIMELLQELKEEYGMSVIFITHDLSVATNFCDRIITMYAGKIVEEAPVE 240
           PTTALDVT+QAQI+ELL+EL  E G ++I ITHD+ V    CD ++ MYAG+ VE+A   
Sbjct: 180 PTTALDVTVQAQIIELLRELNRERGTAIILITHDMGVVAGLCDDVMVMYAGQTVEQASAA 239

Query: 241 EILKTPLHPYTKGLLNS---TLEIGSRGKKLVPIPGNPPNPTKHPSGCKFHPRCSFAMEI 297
            +   P HPYT+GLLN+     +     + L  IPGNPP P +  +GC F PRC++  + 
Sbjct: 240 SLFAAPTHPYTRGLLNALPRLTDSSDDDRPLQTIPGNPPLPGEVGAGCAFAPRCAYCSDQ 299

Query: 298 CQREEPPLVNISENHRV--ACHLIKGE 322
           C++  P LV    + +   ACH   GE
Sbjct: 300 CRQSRPALVAADGDPQALRACHRPVGE 326


Lambda     K      H
   0.320    0.139    0.401 

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: 277
Number of extensions: 13
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: 324
Length of database: 333
Length adjustment: 28
Effective length of query: 296
Effective length of database: 305
Effective search space:    90280
Effective search space used:    90280
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 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