GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Marinobacter adhaerens HP15

Align ABC transporter for D-Mannitol, D-Mannose, and D-Mannose, ATPase component (characterized)
to candidate GFF770 HP15_749 iron(III) ABC transporter, ATP-binding protein

Query= reanno::pseudo13_GW456_L13:PfGW456L13_3039
         (367 letters)



>FitnessBrowser__Marino:GFF770
          Length = 357

 Score =  209 bits (532), Expect = 9e-59
 Identities = 128/354 (36%), Positives = 190/354 (53%), Gaps = 16/354 (4%)

Query: 4   LKIKNLQKGFEGFSIIKGIDLEVNDKEFVVFVGPSGCGKSTLLRLIAGLEEVSGGTIELD 63
           L++ NL  G+ G S++K +   ++  +    +GPSGCGKST+LR +AG   +SGG I L 
Sbjct: 13  LEVNNLSCGYGGDSVVKDVSFALSHGDIGCLLGPSGCGKSTILRALAGFLPLSGGEISLQ 72

Query: 64  GRDIT----EVSPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVAKAEVEKKVSEAAR 119
            + I+     + P KR + MVFQ YAL+PH+++  N+ F L    + KAE  +KV E   
Sbjct: 73  SQAISLPGRTLPPEKRRIGMVFQDYALFPHLTIADNVGFGL--RNLNKAEKRQKVMELLN 130

Query: 120 ILELGPMLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELLRL 179
           ++ L  + +  P +LSGGQ+QRVA+ RA+   P + L DEP SNLDA LR ++ L++  +
Sbjct: 131 VVHLQDLADNYPHELSGGQQQRVALARALAPEPTLILLDEPFSNLDADLRRRLSLDVREI 190

Query: 180 HKELQATMIYVTHDQVEAMTMADKVVVLNGGKIEQVGSPLDLYHQPANLFVAGFLGTPKM 239
            K L  + I VTHDQ EA  M D+V VL  G+I+Q   P +LYH+PAN FVA F+G  + 
Sbjct: 191 LKTLGISAILVTHDQQEAFAMCDQVAVLRDGRIQQWDVPYNLYHEPANRFVASFVG--QG 248

Query: 240 GFLKGKITRVDSQGCEVQLDAGTRVSLPLGGRHLSVGSAVTLGIRPEHLELAKPGDCALQ 299
           GF+ G     D+   E+ +  G R            G+ V + IRP+  ++    D  LQ
Sbjct: 249 GFVPGTALGPDTIESELGVIHGNR------AYKWEPGTLVDVLIRPD--DIVHDPDSDLQ 300

Query: 300 VTADVSERLGSDTFCHVRTASGEALTMRVRGDLASRYGETLSLHLDAQHCHLFD 353
                    G+ T    R +         R  L    GE + + ++A H   F+
Sbjct: 301 PKVVEKTFAGTSTLYRFRCSEDTEFEALFRSHLDFNLGEHVPVRVEADHLIAFE 354


Lambda     K      H
   0.320    0.137    0.389 

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: 324
Number of extensions: 16
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: 367
Length of database: 357
Length adjustment: 29
Effective length of query: 338
Effective length of database: 328
Effective search space:   110864
Effective search space used:   110864
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