GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Cupriavidus basilensis 4G11

Align ABC transporter for D-Mannitol, D-Mannose, and D-Mannose, ATPase component (characterized)
to candidate RR42_RS18590 RR42_RS18590 hypothetical protein

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



>FitnessBrowser__Cup4G11:RR42_RS18590
          Length = 359

 Score =  349 bits (896), Expect = e-101
 Identities = 186/358 (51%), Positives = 248/358 (69%), Gaps = 7/358 (1%)

Query: 1   MANLKIKNLQKGFEGFSIIKGIDLEVNDKEFVVFVGPSGCGKSTLLRLIAGLEEVSGGTI 60
           MA+++I+ +QK F    +I+G+D+++ D +F V VGPSGCGKSTLLR+IAGLEE++ G I
Sbjct: 1   MASVQIRGIQKYFGSTQVIRGVDIDIADGQFTVLVGPSGCGKSTLLRMIAGLEEITTGEI 60

Query: 61  ELDGRDITEVSPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVAKAEVEKKVSEAARI 120
            +  R +  + P +RD+AMVFQ YALYPHM+V  NM+F+L LA   K E+++KV++A+ I
Sbjct: 61  AIGNRVVNRLPPKERDIAMVFQNYALYPHMTVYDNMAFSLKLAKGDKEEIKRKVAKASAI 120

Query: 121 LELGPMLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELLRLH 180
           L L  +LER P+QLSGGQRQRVA+GRAIVR+P++FLFDEPLSNLDA LRVQMR E+  LH
Sbjct: 121 LGLDSLLERYPRQLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVQMRAEIKELH 180

Query: 181 KELQATMIYVTHDQVEAMTMADKVVVLNGGKIEQVGSPLDLYHQPANLFVAGFLGTPKMG 240
           + L+ T +YVTHDQ+EAMTMAD++VV+  G++EQ G PL LY  P NLFVAGF+G+P M 
Sbjct: 181 QRLRTTSVYVTHDQIEAMTMADQIVVMRDGRVEQRGKPLALYDHPDNLFVAGFIGSPAMN 240

Query: 241 FLKGKITRVDSQGCEVQLDAGTRVSLP--LGGRHLSVGSAVTLGIRPEHLELAKPGDCAL 298
           F+ G + R       V+   GTR+  P        + G  V  G+RPEHL L  PG   L
Sbjct: 241 FVPGVLRRSGGDAA-VEFPDGTRLPAPARFDATAGTDGQRVIYGVRPEHLTLGMPGQ-GL 298

Query: 299 QVTADVSERLGSDTFCHVRTASGEALTM-RVRGDLASRYGETLSLHLDAQHCHLFDAD 355
           Q    V E  G++T  + R    E +++ R R D A+  G+ L+L  D QH HLFDAD
Sbjct: 299 QTRVSVVEPTGANTEIYSRFCEAEFISIFRERHDFAA--GDILNLVPDHQHTHLFDAD 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: 385
Number of extensions: 15
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: 359
Length adjustment: 29
Effective length of query: 338
Effective length of database: 330
Effective search space:   111540
Effective search space used:   111540
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