GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lacK in Brucella inopinata BO1

Align LacK, component of Lactose porter (characterized)
to candidate WP_008510203.1 BIBO1_RS16720 sn-glycerol-3-phosphate import ATP-binding protein UgpC

Query= TCDB::Q01937
         (363 letters)



>NCBI__GCF_000182725.1:WP_008510203.1
          Length = 351

 Score =  342 bits (877), Expect = 9e-99
 Identities = 190/368 (51%), Positives = 249/368 (67%), Gaps = 25/368 (6%)

Query: 1   MAEVRLTDIRKSYG-SLEVIKGVNLEVSSGEFVVFVGPSGCGKSTLLRMIAGLEDISSGE 59
           M+++ L ++RKSYG ++EVIKGV+LE++ GEFVV VGPSGCGKSTLLRMIAGLE I+SG 
Sbjct: 1   MSKIVLDNVRKSYGGNIEVIKGVSLEIADGEFVVLVGPSGCGKSTLLRMIAGLESITSGT 60

Query: 60  LTIGGTVMNDVDPSKRGIAMVFQTYALYPHMTVRENMGFALRFAGMAKDEIERRVNAAAK 119
           ++IG  V+N+V+P++R IAMVFQ YALYPHMTVREN+ + L+     K+EIERR+  AAK
Sbjct: 61  ISIGERVVNNVEPAERDIAMVFQNYALYPHMTVRENLAYGLKNRKTPKEEIERRIAKAAK 120

Query: 120 ILELDALMDRKPKALSGGQRQRVAIGRAIVRQPDVFLFDEPLSNLDAELRVHMRVEIARL 179
            LE++  ++RKP+ LSGGQRQRVA+GRAIVR+P  FLFDEPLSNLDA+LRV MRVEI RL
Sbjct: 121 ALEIEQFLERKPRQLSGGQRQRVAMGRAIVREPAAFLFDEPLSNLDAKLRVQMRVEIKRL 180

Query: 180 HKELNATIVYVTHDQVEAMTLADKIVVMRGGIVEQVGAPLALYDDPDNMFVAGFIGSPRM 239
            + L  T VYVTHDQ+EAMT+AD++VV+  G +EQVG P+ LY+ P + FVA FIGSP M
Sbjct: 181 QRSLGTTSVYVTHDQMEAMTMADRLVVLNAGHIEQVGTPIELYEKPASTFVATFIGSPSM 240

Query: 240 NFLPAVVIGQAEGGQVTVALKARPDTQLTVACATPPQGGDAVTVGVRPEHFLPAGSGDT- 298
           N L           Q + +   +P + +T+     P GG   T GVRPE       GD  
Sbjct: 241 NLL-----------QSSESAAWQPGSAITL-----PSGG--YTFGVRPEDIRILEEGDQD 282

Query: 299 ----QLTAHVDVVEHLGNTSYVYAHTVPGEQIIIEQEERRHGGRYGDEIAVGISAKTSFL 354
                    ++ VE +G  SY++A    G+ +I  +   R      + + VG SA    +
Sbjct: 283 ADGFNAQVRIEAVELVGAESYIHAALSDGKPLIF-RVAGRSTHNIDEMVRVGASATDVHI 341

Query: 355 FDASGRRI 362
           F A GRR+
Sbjct: 342 FGADGRRV 349


Lambda     K      H
   0.320    0.137    0.390 

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: 340
Number of extensions: 11
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: 363
Length of database: 351
Length adjustment: 29
Effective length of query: 334
Effective length of database: 322
Effective search space:   107548
Effective search space used:   107548
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 24 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