GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Phaeobacter inhibens BS107

Align Maltose/maltodextrin import ATP-binding protein MalK; EC 7.5.2.1 (characterized)
to candidate GFF729 PGA1_c07440 ABC transporter, ATP binding protein

Query= SwissProt::P19566
         (369 letters)



>FitnessBrowser__Phaeo:GFF729
          Length = 353

 Score =  338 bits (868), Expect = 1e-97
 Identities = 194/366 (53%), Positives = 247/366 (67%), Gaps = 17/366 (4%)

Query: 1   MASVQLRNVTKAWGDVVVSKDINLDIHDGEFVVFVGPSGCGKSTLLRMIAGLETITSGDL 60
           M  V L    K +GDV V  D++L I DGEF VFVGPSGCGKSTLLRMIAGLE  +SG++
Sbjct: 1   MTGVTLAKAVKKYGDVQVIHDVDLSIDDGEFCVFVGPSGCGKSTLLRMIAGLEETSSGNI 60

Query: 61  FIGETRMNDIPPAERGVGMVFQSYALYPHLSVAENMSFGLKLAGAKKEVMNQRVNQVAEV 120
            IG+  +  +  A+RGV MVFQSYALYPH++V +NM FGLK+ G  KE + ++V + + +
Sbjct: 61  HIGDRDVTRLDAADRGVAMVFQSYALYPHMTVEDNMGFGLKMNGHPKEKIREKVAEASRI 120

Query: 121 LQLAHLLERKPKALSGGQRQRVAIGRTLVAEPRVFLLDEPLSNLDAALRVQMRIEISRLH 180
           L+L   L+RKPKALSGGQRQRVAIGR +V  P VFL DEPLSNLDA LRV MR+EI+RLH
Sbjct: 121 LKLDDYLKRKPKALSGGQRQRVAIGRAIVRGPEVFLFDEPLSNLDAELRVDMRVEIARLH 180

Query: 181 KRLGRTMIYVTHDQVEAMTLADKIVVLDAGRVAQVGKPLELYHYPADRFVAGFIGSPKMN 240
           K +G TMIYVTHDQVEAMTLADKIVVL AGRV QVG P+ELY  P +RFVAGFIGSP MN
Sbjct: 181 KEIGATMIYVTHDQVEAMTLADKIVVLRAGRVEQVGSPMELYANPDNRFVAGFIGSPSMN 240

Query: 241 FLPVKVTATAIEQVQVELPNRQ---QIWLPVESRGVQVGANMSLGIRPEHLLPSDIADVT 297
           FL   V    +  V   L NR+    + LP +      G+ + LG+RP+HL  +  AD +
Sbjct: 241 FLEGTVQGDGV--VVPALENRRVATSVALPAD------GSKVLLGLRPQHLSVT-AADSS 291

Query: 298 LEGEVQVVEQLGHETQIHIQIPAIRQNLVYRQNDVVLVEEGATFAIGLPPERCHLFREDG 357
           L  +++  E+LG  +  ++  P   + +V  + D  L  EG   A+G      ++F  DG
Sbjct: 292 LVLDLR--ERLGGVSYDYLSTPTGEKLIVETRGDEAL-PEGTAVALGFDDADAYIF--DG 346

Query: 358 SACRRL 363
           +  +RL
Sbjct: 347 ATEQRL 352


Lambda     K      H
   0.321    0.138    0.396 

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: 359
Number of extensions: 12
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: 369
Length of database: 353
Length adjustment: 29
Effective length of query: 340
Effective length of database: 324
Effective search space:   110160
Effective search space used:   110160
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.

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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