GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potD in Azospirillum brasilense Sp245

Align Putrescine-binding periplasmic protein SpuD (characterized)
to candidate AZOBR_RS08845 AZOBR_RS08845 ABC transporter substrate-binding protein

Query= SwissProt::Q02UB7
         (367 letters)



>FitnessBrowser__azobra:AZOBR_RS08845
          Length = 366

 Score =  320 bits (821), Expect = 3e-92
 Identities = 157/367 (42%), Positives = 237/367 (64%), Gaps = 2/367 (0%)

Query: 2   MKRFGKTLLALTLAGSVAGMAQAADNKVLHVYNWSDYIAPDTLEKFTKETGIKVVYDVYD 61
           MKRF  +++    A ++AG A A   K +++Y W+DY+   TL  FTK TG     D+YD
Sbjct: 1   MKRFALSVIGAVAAIAIAGPALAQAKKPVNIYIWNDYLGESTLADFTKATGYDTKVDLYD 60

Query: 62  SNEVLEAKLLAGKSGYDVVVPS-NSFLAKQIKAGVYQKLDKSKLPNWKNLNKDLMHTLEV 120
           S E+LE K+L GKSGYDV+VP+    L++ I+A V   LDK+K+PN KN++  ++  LE 
Sbjct: 61  SLELLEQKVLVGKSGYDVIVPTAEPTLSRMIQAKVVAPLDKAKIPNLKNVDPKVLKLLEN 120

Query: 121 SDPGNEHAIPYMWGTIGIGYNPDKVKAAFGDNAPVDSWDLVFKPENIQKLKQCGVSFLDS 180
           SDPGN+ A+PY+ GT+GI   P+K+KA   D  P+DSWDL+FKPE  +K+  CG++ +DS
Sbjct: 121 SDPGNKFAVPYLGGTVGIAIIPEKIKAVAPD-VPLDSWDLIFKPEVAKKVAACGITVMDS 179

Query: 181 PTEILPAALHYLGYKPDTDNPKELKAAEELFLKIRPYVTYFHSSKYISDLANGNICVAIG 240
             +++P+ L+YLG  P+++  ++L   E+  L +RPY+  F + + I+ LA G+ CV + 
Sbjct: 180 AIDVIPSVLNYLGLDPNSEKKEDLDKVEKTLLAVRPYIKQFVTGQNINILAGGDACVVMA 239

Query: 241 YSGDIYQAKSRAEEAKNKVTVKYNIPKEGAGSFFDMVAIPKDAENTEGALAFVNFLMKPE 300
           Y+GD  Q  +RAEEAKN V V+Y  PKEG   ++D +AIP DA N EGA A++NF++ P 
Sbjct: 240 YNGDAIQGAARAEEAKNGVKVEYITPKEGVQVWWDTLAIPADAPNKEGAHAYINFILDPA 299

Query: 301 IMAEITDVVQFPNGNAAATPLVSEAIRNDPGIYPSEEVMKKLYTFPDLPAKTQRAMTRSW 360
            +A +++ V + N   A+   V E ++ +P ++  E    KL+    +   T RA TR W
Sbjct: 300 NIAAVSNTVSYANAVPASLASVDEGVKTNPAVFLPENSSLKLFALKSIKQTTDRARTRVW 359

Query: 361 TKIKSGK 367
           TK+K+GK
Sbjct: 360 TKVKTGK 366


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: 427
Number of extensions: 19
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: 367
Length of database: 366
Length adjustment: 30
Effective length of query: 337
Effective length of database: 336
Effective search space:   113232
Effective search space used:   113232
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