GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Pseudomonas stutzeri RCH2

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate GFF1860 Psest_1899 ABC-type sugar transport systems, ATPase components

Query= BRENDA::Q70HW1
         (384 letters)



>FitnessBrowser__psRCH2:GFF1860
          Length = 390

 Score =  324 bits (831), Expect = 2e-93
 Identities = 176/374 (47%), Positives = 236/374 (63%), Gaps = 12/374 (3%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA + L ++ K+Y      T+KD  L I   EF + VGPSGCGK+T +  IAGLE+IT G
Sbjct: 1   MASLELRNVQKSYGNSQIATLKDIALKIDAGEFLILVGPSGCGKSTLMNCIAGLENITGG 60

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            + +    ++   PKDRDIAMVFQ+YALYP M+V  N+AFGLK+RKVP A+I+  V   A
Sbjct: 61  EILVDGEDISQASPKDRDIAMVFQSYALYPTMSVRDNIAFGLKMRKVPAAKIEEEVARVA 120

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
           K+L I  LL+RKP  LSGGQ+QRVA+GRA+ R P+++L DEPLSNLDAKLRV+MR EI+ 
Sbjct: 121 KLLQIEPLLERKPSQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEIKL 180

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           +HQRL+TT +YVTHDQ EAMT+GD++ VM+DGVIQQ  TP  +Y+ P N+FVA FIGSP 
Sbjct: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGVIQQFGTPHEIYNNPANLFVASFIGSPP 240

Query: 241 MNFIRGEIVQ-DG---DAFYFRAPSISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDE 296
           MNF+   I Q DG           S  L LP     +    G   + ++LG+RPE +   
Sbjct: 241 MNFVPLRIRQRDGRWVGVLNSEQGSCELPLP-----ITSDDGLRDRELILGIRPEQI--- 292

Query: 297 EVFMTTYPDSVLQMQVEVVEHMGSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDLN 356
            +      D  L + +EVVE  G +  +  ++       R+ P     VG ++ L  D  
Sbjct: 293 GLAPAGSADFSLAVDIEVVEPTGPDTLVVFTLNQVKACCRLAPDQAPRVGETLNLQFDPR 352

Query: 357 KIHIFDAETEESIG 370
           +  +FDA+T E +G
Sbjct: 353 RALLFDAQTGERLG 366


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: 421
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: 390
Length adjustment: 30
Effective length of query: 354
Effective length of database: 360
Effective search space:   127440
Effective search space used:   127440
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 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