GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Phaeobacter inhibens BS107

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate GFF729 PGA1_c07440 ABC transporter, ATP binding protein

Query= BRENDA::Q70HW1
         (384 letters)



>FitnessBrowser__Phaeo:GFF729
          Length = 353

 Score =  312 bits (800), Expect = 8e-90
 Identities = 184/371 (49%), Positives = 232/371 (62%), Gaps = 21/371 (5%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           M  V L    K Y G  +  + D +L I D EF VFVGPSGCGK+T LRMIAGLE+ + G
Sbjct: 1   MTGVTLAKAVKKY-GDVQ-VIHDVDLSIDDGEFCVFVGPSGCGKSTLLRMIAGLEETSSG 58

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
           N++IGDR V  +   DR +AMVFQ+YALYPHMTV  NM FGLK+   PK +I  +V EA+
Sbjct: 59  NIHIGDRDVTRLDAADRGVAMVFQSYALYPHMTVEDNMGFGLKMNGHPKEKIREKVAEAS 118

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
           +IL +   L RKPKALSGGQRQRVA+GRAIVR P+VFL DEPLSNLDA+LRV MR EI +
Sbjct: 119 RILKLDDYLKRKPKALSGGQRQRVAIGRAIVRGPEVFLFDEPLSNLDAELRVDMRVEIAR 178

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           LH+ +  T+IYVTHDQ EAMT+ D+IVV+R G ++Q  +P  +Y+ P N FVAGFIGSP+
Sbjct: 179 LHKEIGATMIYVTHDQVEAMTLADKIVVLRAGRVEQVGSPMELYANPDNRFVAGFIGSPS 238

Query: 241 MNFIRGEIVQDGDAFYFRAPSISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDEEVFM 300
           MNF+ G +  DG       P++  R    R     A  A G  V+LG+RP+ L       
Sbjct: 239 MNFLEGTVQGDGVV----VPALENR----RVATSVALPADGSKVLLGLRPQHL------S 284

Query: 301 TTYPDSVLQMQVEVVEHMG--SEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDLNKI 358
            T  DS L + +   E +G  S  YL T  G   IV           G++V L  D    
Sbjct: 285 VTAADSSLVLDLR--ERLGGVSYDYLSTPTGEKLIV-ETRGDEALPEGTAVALGFDDADA 341

Query: 359 HIFDAETEESI 369
           +IFD  TE+ +
Sbjct: 342 YIFDGATEQRL 352


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: 384
Number of extensions: 13
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: 384
Length of database: 353
Length adjustment: 30
Effective length of query: 354
Effective length of database: 323
Effective search space:   114342
Effective search space used:   114342
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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