GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potD in Magnetospirillum magneticum AMB-1

Align Putrescine-binding periplasmic protein SpuD (characterized)
to candidate WP_011385005.1 AMB_RS13210 polyamine ABC transporter substrate-binding protein

Query= SwissProt::Q02UB7
         (367 letters)



>NCBI__GCF_000009985.1:WP_011385005.1
          Length = 369

 Score =  363 bits (931), Expect = e-105
 Identities = 197/370 (53%), Positives = 252/370 (68%), Gaps = 8/370 (2%)

Query: 4   RFGKTLLALTL----AGSVAGMAQAADNKVLHVYNWSDYIAPDTLEKFTKETGIKVVYDV 59
           R   T +A++L      SV+G AQAA++KVL+VYNWSDYIAPDTLEKFT  TGIKV YDV
Sbjct: 2   RISFTAVAVSLIAAAVSSVSG-AQAAEDKVLNVYNWSDYIAPDTLEKFTALTGIKVNYDV 60

Query: 60  YDSNEVLEAKLLAGKSGYDVVVPSNS-FLAKQIKAGVYQKLDKSKLPNWKNLNKDLMHTL 118
           YDSNEVL+AKL AGKSGYDVV PS S FLA QIKAG+Y+KLD+SKL N+ NL+  +M TL
Sbjct: 61  YDSNEVLQAKLQAGKSGYDVVFPSASPFLANQIKAGIYRKLDRSKLSNYGNLDAQVMVTL 120

Query: 119 E-VSDPGNEHAIPYMWGTIGIGYNPDKVKAAFGDNAPVDSWDLVFKPENIQKLKQCGVSF 177
              +DPGN +AIPY     G  YN DKV  A G + P+DSW  +F P  + KLK CGVS 
Sbjct: 121 NRAADPGNLYAIPYAISPTGFAYNVDKVAKA-GKDMPLDSWAALFDPAQVAKLKGCGVSL 179

Query: 178 LDSPTEILPAALHYLGYKPDTDNPKELKAAEELFLKIRPYVTYFHSSKYISDLANGNICV 237
           LD+PTE+ PAAL YLG    + +  +LKAA E   K+RP + YFHSSK+I+DLANG+IC+
Sbjct: 180 LDAPTEVFPAALTYLGKNGASLDSADLKAAAEAVTKVRPSIKYFHSSKFINDLANGDICM 239

Query: 238 AIGYSGDIYQAKSRAEEAKNKVTVKYNIPKEGAGSFFDMVAIPKDAENTEGALAFVNFLM 297
           A GY GD+ Q+++RA EA   V +K  IPKEGA    D + IP DA + E A  F++F+M
Sbjct: 240 AHGYVGDLVQSRNRAAEAGKGVNIKIVIPKEGAVINIDSMVIPADAPHPENAHKFIDFMM 299

Query: 298 KPEIMAEITDVVQFPNGNAAATPLVSEAIRNDPGIYPSEEVMKKLYTFPDLPAKTQRAMT 357
           K E+ A  ++   + N    +  L+ + I+ DP I+PSE+V  KLY  P      +R  T
Sbjct: 300 KQEVAAGFSNTTGYGNPIPGSRSLIRKEIQEDPVIFPSEQVTAKLYQVPPADMAKERERT 359

Query: 358 RSWTKIKSGK 367
           R WT +K+G+
Sbjct: 360 RLWTTVKTGR 369


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: 459
Number of extensions: 24
Number of successful extensions: 4
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: 369
Length adjustment: 30
Effective length of query: 337
Effective length of database: 339
Effective search space:   114243
Effective search space used:   114243
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