GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Desulfacinum infernum DSM 9756

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 WP_073037051.1 BUB04_RS03685 ABC transporter ATP-binding protein

Query= TCDB::Q8DT25
         (377 letters)



>NCBI__GCF_900129305.1:WP_073037051.1
          Length = 361

 Score =  201 bits (511), Expect = 3e-56
 Identities = 125/346 (36%), Positives = 192/346 (55%), Gaps = 20/346 (5%)

Query: 1   MTTLKLDNIYKRYP-NAKHYSVENFNLDIHDKEFIVFVGPSGCGKSTTLRMIAGLEDITE 59
           +T  ++ + Y+R+P +   Y+++N +    D      +GPSGCGK+T L +I+GL   T 
Sbjct: 4   ITLQEVAHSYRRHPKDPSDYALKNIDTVWEDGGAYALLGPSGCGKTTMLNIISGLLTPTR 63

Query: 60  GNLYIDDKLMNDASPKDRDIAMVFQNYALYPHMSVYENMAFGLKLRKYKKDDINKRVHEA 119
           G +  DD+ +    P+ R+IA VFQ   LY  MSV++N+AF L+ R      + +RV E 
Sbjct: 64  GRVLYDDRDVTRLPPEQRNIAQVFQFPVLYDTMSVFDNLAFPLRNRGLDPQTVRRRVQEV 123

Query: 120 AEILGLTEFLERKPADLSGGQRQRVAMGRAIVR-DAKVFLMDEPLSNLDAKLRVAMRAEI 178
           AE+L LT  L++K A LS   +Q++++GR +VR D    L DEPL+ +D  L+  +R ++
Sbjct: 124 AEVLDLTADLKKKAAGLSADAKQKISLGRGLVREDVAAILFDEPLTVIDPHLKWHLRRKL 183

Query: 179 AKIHRRIGATTIYVTHDQTEAMTLADRIVIMSATPNPDKTGSIGRIEQIGTPQELYNEPA 238
            +IH R+  T IYVTHDQ EA+T AD++++M            G + Q+GTP EL+ EP 
Sbjct: 184 KEIHERLRLTLIYVTHDQVEALTFADKVLVMYE----------GEVVQMGTPTELFEEPR 233

Query: 239 NKFVAGFIGSPAMNFFEVTVEKERLVNQDGLSLALPQGQEKILEEKGYLGKKVTLGIRPE 298
           +KFV  FIGSP MNF    ++  R V  DG ++ L +   +   EK        LGIRP 
Sbjct: 234 HKFVGYFIGSPGMNFIPCKLDGARAV-FDGAAVPLDEETARRAREK---EGPFELGIRPM 289

Query: 299 DISSDQIVHETFPNASVTADILVSELLGSESMLYVKFGSTEFTARV 344
            +     VH++  +  +   +L  E  G   +L V+  S     R+
Sbjct: 290 YLE----VHDSPGDDRLPVKVLKVEDQGIFRILTVQLASNTLKVRL 331


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: 321
Number of extensions: 17
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: 361
Length adjustment: 30
Effective length of query: 347
Effective length of database: 331
Effective search space:   114857
Effective search space used:   114857
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 Apr 09 2024. 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