GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potD in Marinobacter adhaerens HP15

Align Putrescine-binding periplasmic protein SpuD (characterized)
to candidate GFF961 HP15_940 putrescine ABC transporter, periplasmic putrescine-binding protein

Query= SwissProt::Q02UB7
         (367 letters)



>FitnessBrowser__Marino:GFF961
          Length = 368

 Score =  396 bits (1017), Expect = e-115
 Identities = 199/369 (53%), Positives = 257/369 (69%), Gaps = 3/369 (0%)

Query: 1   MMKRFGKTLLALTLAGSVAGMAQAADNKVLHVYNWSDYIAPDTLEKFTKETGIKVVYDVY 60
           M+K      LA ++A S+   +  A  +V  VYNWSDYIA DTL KFT+ETGIKV+YDVY
Sbjct: 1   MLKLCKPQALAASVALSLCASSAFAAEEV-RVYNWSDYIAEDTLAKFTEETGIKVIYDVY 59

Query: 61  DSNEVLEAKLLAGKSGYDVVVPSNSFLAKQIKAGVYQKLDKSKLPNWKNLNKDLMHTLEV 120
           DSNE+LEA LL+G+SGYD+VVPSN ++AKQI A  +  LD SKLPN  NLN DLM  LE 
Sbjct: 60  DSNEILEAALLSGRSGYDLVVPSNHYVAKQISANAFVALDHSKLPNMSNLNPDLMDDLEK 119

Query: 121 SDPGNEHAIPYMWGTIGIGYNPDKVKAAFGDNAPVDSWDLVFKPENIQKLKQ--CGVSFL 178
            DPG++ A+PY+WGT G GYN  +++   GD+AP DSW LVF PE   KL    CG++ L
Sbjct: 120 VDPGSQFALPYLWGTNGYGYNEGRIQEILGDSAPTDSWALVFDPEVTGKLATGGCGIAML 179

Query: 179 DSPTEILPAALHYLGYKPDTDNPKELKAAEELFLKIRPYVTYFHSSKYISDLANGNICVA 238
           DS  E++ AA+ Y+G  P+++N  ++K   E+   IRP +TYFHSS+YI DLANG++CVA
Sbjct: 180 DSGEEMVRAAMAYIGLDPNSNNADDIKKGGEVIKAIRPNITYFHSSRYIGDLANGDLCVA 239

Query: 239 IGYSGDIYQAKSRAEEAKNKVTVKYNIPKEGAGSFFDMVAIPKDAENTEGALAFVNFLMK 298
            GYSGDI QA +RAEEA+N   ++Y IPKEGA  +FDM+ IP  A N E A   +NFLM+
Sbjct: 240 AGYSGDILQAAARAEEAENGNVIRYTIPKEGAVLWFDMMTIPAGAPNVENAHKLMNFLMR 299

Query: 299 PEIMAEITDVVQFPNGNAAATPLVSEAIRNDPGIYPSEEVMKKLYTFPDLPAKTQRAMTR 358
           PEI+A++T+ V + N N  A   V   I +D  IYP++EVMKKLY     P   QR MTR
Sbjct: 300 PEIIADVTNYVWYANPNKPANEFVDPEILSDTSIYPTDEVMKKLYIMEGRPQDAQRLMTR 359

Query: 359 SWTKIKSGK 367
           +WT +KSG+
Sbjct: 360 TWTNVKSGR 368


Lambda     K      H
   0.315    0.133    0.390 

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: 477
Number of extensions: 20
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: 367
Length of database: 368
Length adjustment: 30
Effective length of query: 337
Effective length of database: 338
Effective search space:   113906
Effective search space used:   113906
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 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