GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1749 in Pseudomonas putida KT2440

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 PP_0878 PP_0878 dipeptide ABC transporter, binding subunit

Query= TCDB::Q9X271
         (324 letters)



>FitnessBrowser__Putida:PP_0878
          Length = 322

 Score =  228 bits (582), Expect = 1e-64
 Identities = 117/299 (39%), Positives = 187/299 (62%), Gaps = 9/299 (3%)

Query: 20  IVKAVDGISYKLNKGESLGIVGESGSGKSVSVLSLLRLINRNGRIVDGEAIFLGKDLLKL 79
           +V+A++G+S++L  G++L +VGESG GKS    +L R +        G     G ++   
Sbjct: 26  LVRALNGVSFELEAGKTLAVVGESGCGKS----TLARALTLIEEPSSGSLQIAGTEVKGA 81

Query: 80  NKEELRNIRGKDISIIFQNPMTSLNPIIRVGIQVMEPIIWHRLMKNEEARERAIELLERV 139
           +K E + +R +D+ ++FQ+P  SLNP  ++G Q+ EP++ +  +   E R++  +++E+V
Sbjct: 82  SKAERKQLR-RDVQMVFQSPYASLNPRQKIGDQLAEPLLINTSLSKAERRDKVQKMMEQV 140

Query: 140 GIPESPKRFLNYPFQFSGGMRQRVMIAMALACHPKLLIADEPTTALDVTIQAQIMELLQE 199
           G+   P+ +  YP  FSGG RQR+ +A A+   PK+L+ADEPT+ALDV+IQAQ++ L  +
Sbjct: 141 GL--RPEHYQRYPHMFSGGQRQRIALARAMMLQPKVLVADEPTSALDVSIQAQVLNLFMD 198

Query: 200 LKEEYGMSVIFITHDLSVATNFCDRIITMYAGKIVEEAPVEEILKTPLHPYTKGLLNSTL 259
           L++E+  + +FI+H+L+V  +  D+++ MY G+  E  P E+I   PLHPYT+ LL++T 
Sbjct: 199 LQKEFNTAYVFISHNLAVVRHVADQVLVMYLGRPAEMGPKEDIYAKPLHPYTQALLSATP 258

Query: 260 EIGSRG-KKLVPIPGNPPNPTKHPSGCKFHPRCSFAMEICQREEPPLVNISENHRVACH 317
            I     K  + I G  PNP   P GC FH RC +A E C +E P L  +S   +VACH
Sbjct: 259 AIHPDPLKPKIRIVGELPNPLNPPDGCAFHKRCPYATERCAKEVPALRQVS-TRQVACH 316


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: 257
Number of extensions: 18
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: 322
Length adjustment: 28
Effective length of query: 296
Effective length of database: 294
Effective search space:    87024
Effective search space used:    87024
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.

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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