GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Desulfacinum infernum DSM 9756

Align Maltose-transporting ATPase (EC 3.6.3.19) (characterized)
to candidate WP_073038605.1 BUB04_RS08650 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::psRCH2:GFF857
         (371 letters)



>NCBI__GCF_900129305.1:WP_073038605.1
          Length = 368

 Score =  317 bits (813), Expect = 3e-91
 Identities = 175/367 (47%), Positives = 237/367 (64%), Gaps = 14/367 (3%)

Query: 1   MASVTLRDICKSYDGTPITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDITSGDL 60
           MA + L  + K +    + R   L + D EFVV VGPSGCGKST LR+IAGLE++TSG++
Sbjct: 1   MAEIKLDQVNKRFKKNWVVRDFTLTVADKEFVVLVGPSGCGKSTTLRMIAGLEEVTSGEI 60

Query: 61  LIDNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRVEAVAEI 120
            I  + VN +PPKDR + MVFQSYALYPHM V +NMAFGL    V + EI RRV+  AEI
Sbjct: 61  SIGGRVVNHVPPKDRDIAMVFQSYALYPHMNVYKNMAFGLMNRGVPRDEIDRRVKQAAEI 120

Query: 121 LQLDKLLERKPKDLSGGQRQRVAIGRTMVREPKVFLFDEPLSNLDAFLRVQMRIEIARLH 180
           L +  LL+R+P  LSGGQRQRVA+GR +VR+P+ FLFDEPLSNLDA LRVQMR E+A+LH
Sbjct: 121 LGISDLLQRRPAQLSGGQRQRVAMGRAIVRDPQAFLFDEPLSNLDAKLRVQMRAELAKLH 180

Query: 181 QRIRSTMIYVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGFLGSPQMN 240
           +R++ST++YVTHDQ+EAMTLAD+IVV+  G+I QVG PL +Y  P NRFVAGF+GSP MN
Sbjct: 181 ERLQSTIVYVTHDQIEAMTLADRIVVMKDGKIMQVGPPLEVYERPANRFVAGFIGSPSMN 240

Query: 241 FVEVRAISASPETVTIELPSGYPLTLPVDGSAVSPGD---PLTLGIRPEHF------VMP 291
           F++VR +  + + + ++  S + L +P   +    G    P+  GIRPE         +P
Sbjct: 241 FLDVRLVEEAGD-LWVDGES-FRLKVPRHRAPAFRGHVNRPVIFGIRPEDVKERPGDALP 298

Query: 292 DEADFTFHGQITVAERLGQYNLLYLTLERLQDVITLCVDGNLRVTEGETFAAGLKADKCH 351
           +  +     ++ V E +G   ++  T+       T  +  N+ V   +     +  +K H
Sbjct: 299 EGVE-PLRAEVDVREPIGSEVIITATVG--SHAFTARISPNVAVRVHDPIDLAVNMNKMH 355

Query: 352 LFRENGE 358
           LF    E
Sbjct: 356 LFDPESE 362


Lambda     K      H
   0.322    0.139    0.405 

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: 405
Number of extensions: 15
Number of successful extensions: 1
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: 371
Length of database: 368
Length adjustment: 30
Effective length of query: 341
Effective length of database: 338
Effective search space:   115258
Effective search space used:   115258
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 (21.9 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