GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Sm in Cupriavidus basilensis 4G11

Align MalK, component of Maltose/Maltotriose/maltodextrin (up to 7 glucose units) transporters MalXFGK (MsmK (3.A.1.1.28) can probably substitute for MalK; Webb et al., 2008) (characterized)
to candidate RR42_RS18590 RR42_RS18590 hypothetical protein

Query= TCDB::Q8DT25
         (377 letters)



>FitnessBrowser__Cup4G11:RR42_RS18590
          Length = 359

 Score =  311 bits (797), Expect = 2e-89
 Identities = 176/376 (46%), Positives = 236/376 (62%), Gaps = 25/376 (6%)

Query: 1   MTTLKLDNIYKRYPNAKHYSVENFNLDIHDKEFIVFVGPSGCGKSTTLRMIAGLEDITEG 60
           M ++++  I K + + +   +   ++DI D +F V VGPSGCGKST LRMIAGLE+IT G
Sbjct: 1   MASVQIRGIQKYFGSTQ--VIRGVDIDIADGQFTVLVGPSGCGKSTLLRMIAGLEEITTG 58

Query: 61  NLYIDDKLMNDASPKDRDIAMVFQNYALYPHMSVYENMAFGLKLRKYKKDDINKRVHEAA 120
            + I ++++N   PK+RDIAMVFQNYALYPHM+VY+NMAF LKL K  K++I ++V +A+
Sbjct: 59  EIAIGNRVVNRLPPKERDIAMVFQNYALYPHMTVYDNMAFSLKLAKGDKEEIKRKVAKAS 118

Query: 121 EILGLTEFLERKPADLSGGQRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVAMRAEIAK 180
            ILGL   LER P  LSGGQRQRVAMGRAIVRD +VFL DEPLSNLDAKLRV MRAEI +
Sbjct: 119 AILGLDSLLERYPRQLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVQMRAEIKE 178

Query: 181 IHRRIGATTIYVTHDQTEAMTLADRIVIMSATPNPDKTGSIGRIEQIGTPQELYNEPANK 240
           +H+R+  T++YVTHDQ EAMT+AD+IV+M            GR+EQ G P  LY+ P N 
Sbjct: 179 LHQRLRTTSVYVTHDQIEAMTMADQIVVMRD----------GRVEQRGKPLALYDHPDNL 228

Query: 241 FVAGFIGSPAMNFFEVTVEKE----RLVNQDGLSLALPQGQEKILEEKGYLGKKVTLGIR 296
           FVAGFIGSPAMNF    + +      +   DG  L  P    +     G  G++V  G+R
Sbjct: 229 FVAGFIGSPAMNFVPGVLRRSGGDAAVEFPDGTRLPAP---ARFDATAGTDGQRVIYGVR 285

Query: 297 PEDISSDQIVHETFPNASVTADILVSELLGSESMLYVKFGSTEFTARVNARDSHSPGEKV 356
           PE ++         P   +   + V E  G+ + +Y +F   EF +    R   + G+ +
Sbjct: 286 PEHLTLG------MPGQGLQTRVSVVEPTGANTEIYSRFCEAEFISIFRERHDFAAGDIL 339

Query: 357 QLTFNIAKGHFFDLET 372
            L  +    H FD ++
Sbjct: 340 NLVPDHQHTHLFDADS 355


Lambda     K      H
   0.318    0.135    0.379 

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: 366
Number of extensions: 22
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: 377
Length of database: 359
Length adjustment: 30
Effective length of query: 347
Effective length of database: 329
Effective search space:   114163
Effective search space used:   114163
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