GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Dyella japonica UNC79MFTsu3.2

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate N515DRAFT_4212 N515DRAFT_4212 multiple sugar transport system ATP-binding protein

Query= BRENDA::Q70HW1
         (384 letters)



>FitnessBrowser__Dyella79:N515DRAFT_4212
          Length = 364

 Score =  371 bits (952), Expect = e-107
 Identities = 200/372 (53%), Positives = 258/372 (69%), Gaps = 19/372 (5%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA+V L+ + K YP      V + + +I D E  V VGPSGCGKTT LRMIAGLE I+ G
Sbjct: 1   MAKVRLDKLRKVYPNG-HVGVAEASFEIADGELLVLVGPSGCGKTTLLRMIAGLESISGG 59

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            L IG+R VND+ PKDRDIAMVFQNYALYPHMTV +N+ FGLKLR  PKAEI+RRV EAA
Sbjct: 60  TLSIGERVVNDIAPKDRDIAMVFQNYALYPHMTVAENLGFGLKLRGQPKAEIERRVAEAA 119

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
           ++L++   LD +P ALSGGQRQRVALGRA+VR+P+VFL+DEPLSNLDAKLR+ MR EI +
Sbjct: 120 RMLELEQRLDSRPAALSGGQRQRVALGRALVRDPKVFLLDEPLSNLDAKLRLSMRVEIAR 179

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           +HQRL+ T++YVTHDQ EAMT+G RIVV+  GVIQQ DTP  +Y  P N+FVAGF+GSPA
Sbjct: 180 IHQRLKATMVYVTHDQIEAMTLGQRIVVLNGGVIQQIDTPMNLYDTPANLFVAGFLGSPA 239

Query: 241 MNFIRGEIVQDGDAFYFRAPSISLRLPEGR--YGVLKASGAI----GKPVVLGVRPEDLH 294
           MN +RG + +DG           L +P+G    G L    A+     + +V+G+RPEDL 
Sbjct: 240 MNLLRGILYRDG--------GWKLAMPQGELVLGELPQGAALEAWRDRDIVVGLRPEDL- 290

Query: 295 DEEVFMTTYPDSVLQMQVEVVEHMGSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAID 354
              +       + L  Q+EVVE +G+EV+L+   G   +V+R+ PR +   GS++     
Sbjct: 291 ---LLCADAAGAALAAQLEVVEPVGNEVFLNLRHGELALVSRMPPRELPAPGSTLHFGFA 347

Query: 355 LNKIHIFDAETE 366
             ++H FDA+ E
Sbjct: 348 PERLHFFDAKGE 359


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: 447
Number of extensions: 18
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: 384
Length of database: 364
Length adjustment: 30
Effective length of query: 354
Effective length of database: 334
Effective search space:   118236
Effective search space used:   118236
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: 50 (23.9 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