GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Desulfovibrio vulgaris Miyazaki F

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate 8499890 DvMF_0655 ABC transporter related (RefSeq)

Query= BRENDA::Q70HW1
         (384 letters)



>FitnessBrowser__Miya:8499890
          Length = 350

 Score =  279 bits (714), Expect = 7e-80
 Identities = 163/350 (46%), Positives = 216/350 (61%), Gaps = 21/350 (6%)

Query: 21  VKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEGNLYIGDRRVNDVPPKDRDIA 80
           V D + +++     V +GPSGCGK+TTLR+IAGLE +T G + IG+R V  +PP  R +A
Sbjct: 19  VDDVSFEVEQGTMLVLLGPSGCGKSTTLRLIAGLESVTSGRIMIGERDVTHLPPAQRQLA 78

Query: 81  MVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAAKILDIAHLLDRKPKALSGGQ 140
           MVFQ+YAL+PH+TV +N+ FGL +RKVP+AE ++R+  A  IL ++ LL RKP  LSGGQ
Sbjct: 79  MVFQSYALFPHLTVRENILFGLTVRKVPEAEREKRLTRAVDILGLSALLQRKPGELSGGQ 138

Query: 141 RQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRKLHQRLQTTVIYVTHDQTEAM 200
           +QRVALGRA+V E  V LMDEPLSNLDAKLR +MR EIR L Q L  T++YVTHDQTEAM
Sbjct: 139 QQRVALGRALVAEAAVCLMDEPLSNLDAKLRHEMRREIRALQQTLGMTMVYVTHDQTEAM 198

Query: 201 TMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPAMNFIRGEIVQDGDAFYFRAP 260
           +M DRI++M+ G I Q  TP  +YS+P   F   FIG+P MN +R   + D       A 
Sbjct: 199 SMADRIILMQGGRIVQNATPSELYSRPATTFAGNFIGTPPMNLVR---LDDARGSVCVAG 255

Query: 261 SISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDEEVFMTTYPDSVLQMQVEVVEHMGS 320
           S S     G   V+ ++       VLG+RPE +          P+   +  VE VE++GS
Sbjct: 256 SRS-----GTVSVVDSA-----DYVLGIRPEHIR-------IVPEG-WRAVVESVEYLGS 297

Query: 321 EVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDLNKIHIFDAETEESIG 370
              L   +G   +   V+      VG+ + L      IHIFDA+T E  G
Sbjct: 298 GSVLGCRVGGEELSVVVDGVPTIAVGAEIYLHCPDEHIHIFDAKTGERRG 347


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: 14
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: 350
Length adjustment: 30
Effective length of query: 354
Effective length of database: 320
Effective search space:   113280
Effective search space used:   113280
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