GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Desulfacinum infernum DSM 9756

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_073037051.1 BUB04_RS03685 ABC transporter ATP-binding protein

Query= BRENDA::Q70HW1
         (384 letters)



>NCBI__GCF_900129305.1:WP_073037051.1
          Length = 361

 Score =  206 bits (523), Expect = 1e-57
 Identities = 127/344 (36%), Positives = 194/344 (56%), Gaps = 20/344 (5%)

Query: 1   MARVLLE---HIYKTYPGQ-TEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLED 56
           MAR+ L+   H Y+ +P   ++  +K+ +   +D      +GPSGCGKTT L +I+GL  
Sbjct: 1   MARITLQEVAHSYRRHPKDPSDYALKNIDTVWEDGGAYALLGPSGCGKTTMLNIISGLLT 60

Query: 57  ITEGNLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRV 116
            T G +   DR V  +PP+ R+IA VFQ   LY  M+V+ N+AF L+ R +    + RRV
Sbjct: 61  PTRGRVLYDDRDVTRLPPEQRNIAQVFQFPVLYDTMSVFDNLAFPLRNRGLDPQTVRRRV 120

Query: 117 QEAAKILDIAHLLDRKPKALSGGQRQRVALGRAIVREP-QVFLMDEPLSNLDAKLRVQMR 175
           QE A++LD+   L +K   LS   +Q+++LGR +VRE     L DEPL+ +D  L+  +R
Sbjct: 121 QEVAEVLDLTADLKKKAAGLSADAKQKISLGRGLVREDVAAILFDEPLTVIDPHLKWHLR 180

Query: 176 AEIRKLHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGF 235
            +++++H+RL+ T+IYVTHDQ EA+T  D+++VM +G + Q  TP  ++ +P++ FV  F
Sbjct: 181 RKLKEIHERLRLTLIYVTHDQVEALTFADKVLVMYEGEVVQMGTPTELFEEPRHKFVGYF 240

Query: 236 IGSPAMNFIRGEIVQDGDAFYFRAPSISLRLPEGRYGVLKASGAIGKPVVLGVRPE--DL 293
           IGSP MNFI  ++  DG    F   ++ L     R    K       P  LG+RP   ++
Sbjct: 241 IGSPGMNFIPCKL--DGARAVFDGAAVPLDEETARRAREKEG-----PFELGIRPMYLEV 293

Query: 294 HDEEVFMTTYPDSVLQMQVEVVEHMGSEVYLHTSIGPNTIVARV 337
           HD         D  L ++V  VE  G    L   +  NT+  R+
Sbjct: 294 HDSP------GDDRLPVKVLKVEDQGIFRILTVQLASNTLKVRL 331


Lambda     K      H
   0.321    0.138    0.395 

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: 335
Number of extensions: 18
Number of successful extensions: 2
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: 384
Length of database: 361
Length adjustment: 30
Effective length of query: 354
Effective length of database: 331
Effective search space:   117174
Effective search space used:   117174
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 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