GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potD in Sinorhizobium meliloti 1021

Align Putrescine-binding periplasmic protein SpuD (characterized)
to candidate SMc00770 SMc00770 putrescine-binding periplasmic protein

Query= SwissProt::Q02UB7
         (367 letters)



>FitnessBrowser__Smeli:SMc00770
          Length = 364

 Score =  388 bits (996), Expect = e-112
 Identities = 194/368 (52%), Positives = 260/368 (70%), Gaps = 5/368 (1%)

Query: 1   MMKRFGKTLLALTLAGSVAGMAQAADNKVLHVYNWSDYIAPDTLEKFTKETGIKVVYDVY 60
           M K    TL    LAGS   +   A  +V++VYNWSDYI    LE+FTKETGIKVVYDV+
Sbjct: 1   MSKLIVATLTTAVLAGST--ILAFAQERVVNVYNWSDYIDDSILEEFTKETGIKVVYDVF 58

Query: 61  DSNEVLEAKLLAGKSGYDVVVPSNSFLAKQIKAGVYQKLDKSKLPNWKNLNKDLMHTLEV 120
           DSNE+LE KLLAG SGYDVVVP+  FL +QI AGV+QKLDKSKLPN  N+   +M     
Sbjct: 59  DSNEILETKLLAGGSGYDVVVPTAYFLQRQIAAGVFQKLDKSKLPNISNMWDMVMERTAQ 118

Query: 121 SDPGNEHAIPYMWGTIGIGYNPDKVKAAFG-DNAPVDSWDLVFKPENIQKLKQCGVSFLD 179
            DPGNE+A+ YMWGT GIGYN +K+K   G D  P  +WD++F PE   K K CG+  LD
Sbjct: 119 YDPGNEYAVDYMWGTTGIGYNVEKMKEILGTDEKP--NWDVIFDPEIAAKFKDCGIHLLD 176

Query: 180 SPTEILPAALHYLGYKPDTDNPKELKAAEELFLKIRPYVTYFHSSKYISDLANGNICVAI 239
           SPT+I+P+AL YLG  PD+ +  +L+ A +L +K+RP +  FHSS+YI+ LANG+IC+A+
Sbjct: 177 SPTDIMPSALAYLGLNPDSHDQADLEKAADLLMKVRPNIRKFHSSEYINALANGDICLAV 236

Query: 240 GYSGDIYQAKSRAEEAKNKVTVKYNIPKEGAGSFFDMVAIPKDAENTEGALAFVNFLMKP 299
           G+SGD++QA+ RA EAK  VTV Y+IP++GA  +FDM+AIP DA +   A  F+N++MKP
Sbjct: 237 GFSGDVFQARDRAAEAKAGVTVDYSIPEQGAQMWFDMLAIPADAPHVAEAHEFINYMMKP 296

Query: 300 EIMAEITDVVQFPNGNAAATPLVSEAIRNDPGIYPSEEVMKKLYTFPDLPAKTQRAMTRS 359
           E++A+ ++ V + NGN A+   + + +  D  IYPS+ VM+KL+T     AK QR +TR 
Sbjct: 297 EVIAKASNYVFYANGNKASQQFLDKEVLEDTAIYPSDAVMQKLFTTTPFEAKEQRVLTRL 356

Query: 360 WTKIKSGK 367
           WT+I +G+
Sbjct: 357 WTRIVTGQ 364


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: 437
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: 364
Length adjustment: 30
Effective length of query: 337
Effective length of database: 334
Effective search space:   112558
Effective search space used:   112558
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