GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potD in Paraburkholderia bryophila 376MFSha3.1

Align Putrescine-binding periplasmic protein (characterized)
to candidate H281DRAFT_05180 H281DRAFT_05180 putrescine transport system substrate-binding protein

Query= SwissProt::P31133
         (370 letters)



>FitnessBrowser__Burk376:H281DRAFT_05180
          Length = 366

 Score =  383 bits (983), Expect = e-111
 Identities = 182/366 (49%), Positives = 258/366 (70%), Gaps = 2/366 (0%)

Query: 6   KKWLSGLVAGALMAVSVG-TLAAEQKTLHIYNWSDYIAPDTVANFEKETGIKVVYDVFDS 64
           K+ + G VA  ++  +   T AA+   L++YNWSDYIA DT+ NF K+TG++V YD +DS
Sbjct: 2   KRRVVGQVAALVLCAAPWLTAAAKDTQLNVYNWSDYIAKDTIPNFTKQTGVQVKYDNYDS 61

Query: 65  NEVLEGKLMAGSTGFDLVVPSASFLERQLTAGVFQPLDKSKLPEWKNLDPELLKLVAKHD 124
           ++ L+ KL+ G++G+D+VVP++++  +Q+ AG+F PLDKSKLP  K LDP L+ LVA  D
Sbjct: 62  DDTLQAKLLTGNSGYDIVVPTSNYAGKQIAAGIFSPLDKSKLPNLKYLDPSLMSLVAGAD 121

Query: 125 PDNKFAMPYMWATTGIGYNVDKVKAVLGENAPVDSWDLILKPENLEKLKSCGVSFLDAPE 184
           PDNKF +P+ + TTG+GYNV K + +LG+N P+D+WD++ KPEN+ KLK+CGVS LDAP+
Sbjct: 122 PDNKFTVPWAYGTTGLGYNVTKAQQILGKNVPLDNWDILFKPENISKLKACGVSVLDAPD 181

Query: 185 EVFATVLNYLGKDPNSTKADDYTGPATDLLLKLRPNIRYFHSSQYINDLANGDICVAIGW 244
           ++FA  L+Y+GKDP ST   DY   A  +L K+RP I  F+SS YINDL  GD+C A GW
Sbjct: 182 QMFAAALHYIGKDPMSTNPADYRA-ALAMLKKIRPYITQFNSSGYINDLVGGDVCFAYGW 240

Query: 245 AGDVWQASNRAKEAKNGVNVSFSIPKEGAMAFFDVFAMPADAKNKDEAYQFLNYLLRPDV 304
           +GDV  A +RA EAK    + + IPK GA  +FDV A+P DAK+K+ A +++NY+  P V
Sbjct: 241 SGDVVIAKHRAIEAKKAYKIEYYIPKGGAPVWFDVMAIPKDAKHKEAALEWINYIETPQV 300

Query: 305 VAHISDHVFYANANKAATPLVSAEVRENPGIYPPADVRAKLFTLKVQDPKIDRVRTRAWT 364
            A I++ V+Y +AN  A   V  +V  +P +YPP DV   LF LK   P++ R++TR WT
Sbjct: 301 HAAITNAVYYPSANLEARKYVDKDVANDPAVYPPPDVIKTLFLLKPLPPEVQRLQTRLWT 360

Query: 365 KVKSGK 370
           + KSG+
Sbjct: 361 EFKSGR 366


Lambda     K      H
   0.317    0.133    0.400 

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: 473
Number of extensions: 16
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: 370
Length of database: 366
Length adjustment: 30
Effective length of query: 340
Effective length of database: 336
Effective search space:   114240
Effective search space used:   114240
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: 41 (21.6 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