GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Halomonas desiderata SP1

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_086510784.1 BZY95_RS15425 ABC transporter ATP-binding protein

Query= BRENDA::Q70HW1
         (384 letters)



>NCBI__GCF_002151265.1:WP_086510784.1
          Length = 373

 Score =  337 bits (865), Expect = 2e-97
 Identities = 182/374 (48%), Positives = 246/374 (65%), Gaps = 7/374 (1%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA + + ++ K +   +E  +KD +L I   EF + VGPSGCGK+T +  IAGLE +T G
Sbjct: 1   MAALEINNVCKDFG--SEQVLKDVSLAIDSGEFLILVGPSGCGKSTLMNAIAGLEPVTSG 58

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            + I    V    P +RDIAMVFQ+YALYP MTV QN++FGL++RKVPKAE +  V+  A
Sbjct: 59  EIRIAGESVTWQTPAERDIAMVFQSYALYPSMTVRQNISFGLEMRKVPKAEREAAVERVA 118

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
            +L I HLL+RKP  LSGGQRQRVA+GRA+ REP+V+L DEPLSNLDAKLRV MR EI+K
Sbjct: 119 DLLQIGHLLERKPSQLSGGQRQRVAMGRALAREPKVYLFDEPLSNLDAKLRVDMRTEIKK 178

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           LHQRL TT++YVTHDQ EAMT+ D I VMRDG I Q  +P  VY+ P ++FVAGF+GSP+
Sbjct: 179 LHQRLGTTIVYVTHDQIEAMTLADCIAVMRDGRILQLGSPDEVYNDPVDLFVAGFMGSPS 238

Query: 241 MNFIRGEIVQDGDAFYFRAPS---ISLRLPEGRYGVLKASG-AIGKPVVLGVRPEDLHDE 296
           MNFI   +V    A+  R  +    +L LP  +     A G  +G+ V+LG+RPE   ++
Sbjct: 239 MNFISATLVGGSGAYRLRVETPGEETLELPWPQERETPALGEKVGERVILGLRPEHFTED 298

Query: 297 EVFMTTYPDSV-LQMQVEVVEHMGSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDL 355
           +  +  Y + V L  ++ VVE  G+++ L   +G     ARV P+     G  + L ID+
Sbjct: 299 DARLGEYAEGVALTPRITVVEPTGADILLQLKLGDGEATARVGPKCRVKAGERLTLRIDM 358

Query: 356 NKIHIFDAETEESI 369
            +  +FD ETE+ +
Sbjct: 359 GRAVMFDRETEKRL 372


Lambda     K      H
   0.321    0.138    0.395 

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: 400
Number of extensions: 10
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: 384
Length of database: 373
Length adjustment: 30
Effective length of query: 354
Effective length of database: 343
Effective search space:   121422
Effective search space used:   121422
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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