GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lacK in Herbaspirillum seropedicae SmR1

Align LacK, component of Lactose porter (characterized)
to candidate HSERO_RS22750 HSERO_RS22750 sugar ABC transporter ATP-binding protein

Query= TCDB::Q01937
         (363 letters)



>FitnessBrowser__HerbieS:HSERO_RS22750
          Length = 377

 Score =  363 bits (932), Expect = e-105
 Identities = 200/366 (54%), Positives = 254/366 (69%), Gaps = 8/366 (2%)

Query: 1   MAEVRLTDIRKSY-GSLEVIKGVNLEVSSGEFVVFVGPSGCGKSTLLRMIAGLEDISSGE 59
           MA V +  +RK+Y G  +V+ G+NL++  GEF V VGPSGCGKSTLLRM+ GLE+IS GE
Sbjct: 1   MAHVNIKQLRKTYDGRADVLAGLNLDIRDGEFCVLVGPSGCGKSTLLRMLCGLEEISGGE 60

Query: 60  LTIGGTVMNDVDPSKRGIAMVFQTYALYPHMTVRENMGFALRFAGMAKDEIERRVNAAAK 119
           L IGG V+N + P++RGIAMVFQ+YALYPHM V +NM F L+ AG +K +I+ R+  AA 
Sbjct: 61  LAIGGQVVNHLPPAERGIAMVFQSYALYPHMNVYKNMAFGLKVAGNSKSDIDARIRHAAA 120

Query: 120 ILELDALMDRKPKALSGGQRQRVAIGRAIVRQPDVFLFDEPLSNLDAELRVHMRVEIARL 179
           IL++D L+ R P+ LSGGQRQRVAIGRAIVRQP +FLFDEPLSNLDA LRV  R+EIA+L
Sbjct: 121 ILKIDHLLQRLPRELSGGQRQRVAIGRAIVRQPRLFLFDEPLSNLDAALRVQTRLEIAKL 180

Query: 180 HKELNATIVYVTHDQVEAMTLADKIVVMRGGIVEQVGAPLALYDDPDNMFVAGFIGSPRM 239
           H++L ATIVYVTHDQVEAMTL DKIVVM  G ++Q G PL LY  P N+FVAGFIGSP+M
Sbjct: 181 HRQLAATIVYVTHDQVEAMTLGDKIVVMHEGRIQQAGTPLELYQQPQNLFVAGFIGSPKM 240

Query: 240 NFLPAVVIGQAEGG-QVTVALKARPDTQLTVACATPPQGGDAVTVGVRPEHFLPAGSGDT 298
           NF   VV    + G QV +A   R    +     TP   G AVT+G+R E  +  G GD 
Sbjct: 241 NFFQGVVTRCDDSGVQVEIAGGLRLLADVDPLGVTP---GAAVTLGLRAEQ-IREGLGDG 296

Query: 299 Q-LTAHVDVVEHLGNTSYVYAHTVPGEQIIIEQEERRHGGRYGDEIAVGISAKTSFLFDA 357
           Q L   V++VEHLG  +++Y     G  I++  +  R+    G  IA+ + +    LFDA
Sbjct: 297 QPLHGVVNLVEHLGEANFLYVTLDGGHDIVVRGDGNRNVD-IGQPIALSVHSHAFHLFDA 355

Query: 358 SGRRIR 363
            G+ +R
Sbjct: 356 QGQALR 361


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: 420
Number of extensions: 9
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: 377
Length adjustment: 30
Effective length of query: 333
Effective length of database: 347
Effective search space:   115551
Effective search space used:   115551
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