GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Bb in Shewanella amazonensis SB2B

Align ABC-type maltose transport, ATP binding protein (characterized, see rationale)
to candidate 6936480 Sama_0668 iron(III) ABC transporter, ATP-binding protein (RefSeq)

Query= uniprot:Q6MNM2
         (347 letters)



>FitnessBrowser__SB2B:6936480
          Length = 341

 Score =  191 bits (484), Expect = 3e-53
 Identities = 111/324 (34%), Positives = 181/324 (55%), Gaps = 33/324 (10%)

Query: 1   MAKIQFSNIKKSFGSADVLKGIDLDIAPGEFLVLVGPSGCGKSTLLRTLAGLESADSGTI 60
           M+ +    +   +    VL+G++L +  GE   L+GPSGCGK+TLLRT+AGL+   +G+I
Sbjct: 1   MSTLSIQGLHSDYRGEQVLRGLNLTLTQGEITALLGPSGCGKTTLLRTIAGLQDISAGSI 60

Query: 61  SIDGKKIND----IEPQNRDIAMVFQSYALYPHMTVAENMGFGLKLKNLAAAEITKRVNE 116
           +I+GK ++     + P+ R I M+FQ YAL+PH+TVA+N+ FG++  +  +  +  R+ E
Sbjct: 61  AINGKTVSADGCFVAPEKRSIGMIFQDYALFPHLTVADNILFGVRQLDKQSRSV--RLEE 118

Query: 117 ISELLQIKHLLDRKPKELSGGQRQRVALGRALSRQTPVILFDEPLSNLDAHLRSQMRLEI 176
           +  L++++ L  R P ELSGGQ+QRV++ RAL+ +  ++L DEP SN+DA +R  + LEI
Sbjct: 119 MLSLVKLEGLGKRYPHELSGGQQQRVSIARALAYEPDLLLLDEPFSNIDAQVRRALMLEI 178

Query: 177 KRLHHNSKSTMIYVTHDQMEATTLGDRIAVLKDGVIEQIGTPSEIYHRPKNTFIATFIGS 236
           + +      + ++VTH + EA    D +A+ + G I Q G P  +Y  P   ++A F+G+
Sbjct: 179 RAILKARNVSAVFVTHSKDEAFAFADTLALFEAGRIVQHGIPETLYQSPNTPYVADFLGA 238

Query: 237 PEMNFLEG--------AVLEKIPWPEARKADQILG---IRPDAFALNQGPLGTQE----- 280
              N+L+         + L   P P+  KA    G   +RP+   +     G  E     
Sbjct: 239 --SNYLDVRLEAGQLISTLGAFPLPQDFKAASETGRWLLRPEQLLIEARADGAGEILERR 296

Query: 281 ---------VALGDFQIDISENLG 295
                    V LG+  +DI  +LG
Sbjct: 297 FLGNGCHYLVRLGEQVLDIHSHLG 320


Lambda     K      H
   0.318    0.136    0.383 

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: 280
Number of extensions: 8
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: 347
Length of database: 341
Length adjustment: 29
Effective length of query: 318
Effective length of database: 312
Effective search space:    99216
Effective search space used:    99216
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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