GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Halomonas desiderata SP1

Align Maltose/maltodextrin import ATP-binding protein MalK; EC 7.5.2.1 (characterized)
to candidate WP_086510784.1 BZY95_RS15425 ABC transporter ATP-binding protein

Query= SwissProt::P19566
         (369 letters)



>NCBI__GCF_002151265.1:WP_086510784.1
          Length = 373

 Score =  307 bits (787), Expect = 3e-88
 Identities = 163/331 (49%), Positives = 219/331 (66%), Gaps = 13/331 (3%)

Query: 1   MASVQLRNVTKAWGDVVVSKDINLDIHDGEFVVFVGPSGCGKSTLLRMIAGLETITSGDL 60
           MA++++ NV K +G   V KD++L I  GEF++ VGPSGCGKSTL+  IAGLE +TSG++
Sbjct: 1   MAALEINNVCKDFGSEQVLKDVSLAIDSGEFLILVGPSGCGKSTLMNAIAGLEPVTSGEI 60

Query: 61  FIGETRMNDIPPAERGVGMVFQSYALYPHLSVAENMSFGLKLAGAKKEVMNQRVNQVAEV 120
            I    +    PAER + MVFQSYALYP ++V +N+SFGL++    K      V +VA++
Sbjct: 61  RIAGESVTWQTPAERDIAMVFQSYALYPSMTVRQNISFGLEMRKVPKAEREAAVERVADL 120

Query: 121 LQLAHLLERKPKALSGGQRQRVAIGRTLVAEPRVFLLDEPLSNLDAALRVQMRIEISRLH 180
           LQ+ HLLERKP  LSGGQRQRVA+GR L  EP+V+L DEPLSNLDA LRV MR EI +LH
Sbjct: 121 LQIGHLLERKPSQLSGGQRQRVAMGRALAREPKVYLFDEPLSNLDAKLRVDMRTEIKKLH 180

Query: 181 KRLGRTMIYVTHDQVEAMTLADKIVVLDAGRVAQVGKPLELYHYPADRFVAGFIGSPKMN 240
           +RLG T++YVTHDQ+EAMTLAD I V+  GR+ Q+G P E+Y+ P D FVAGF+GSP MN
Sbjct: 181 QRLGTTIVYVTHDQIEAMTLADCIAVMRDGRILQLGSPDEVYNDPVDLFVAGFMGSPSMN 240

Query: 241 FLPVK-VTATAIEQVQVELPNRQQIWLP------VESRGVQVGANMSLGIRPEHLLPSD- 292
           F+    V  +   +++VE P  + + LP        + G +VG  + LG+RPEH    D 
Sbjct: 241 FISATLVGGSGAYRLRVETPGEETLELPWPQERETPALGEKVGERVILGLRPEHFTEDDA 300

Query: 293 -----IADVTLEGEVQVVEQLGHETQIHIQI 318
                   V L   + VVE  G +  + +++
Sbjct: 301 RLGEYAEGVALTPRITVVEPTGADILLQLKL 331


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: 364
Number of extensions: 15
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: 373
Length adjustment: 30
Effective length of query: 339
Effective length of database: 343
Effective search space:   116277
Effective search space used:   116277
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 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