GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Cereibacter sphaeroides ATCC 17029

Align ABC transporter for D-mannitol and D-mannose, ATPase component (characterized)
to candidate WP_011841069.1 RSPH17029_RS07670 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::pseudo3_N2E3:AO353_25895
         (367 letters)



>NCBI__GCF_000015985.1:WP_011841069.1
          Length = 369

 Score =  330 bits (845), Expect = 5e-95
 Identities = 182/356 (51%), Positives = 242/356 (67%), Gaps = 8/356 (2%)

Query: 1   MAHLKIKNLQKGFEGFSIIKGIDLEVNDREFVVFVGPSGCGKSTLLRLIAGLEEVTAGTI 60
           MA LK+  ++K +    +++ IDL +   E +VFVGPSGCGKSTLLR+IAGLE +T GT+
Sbjct: 1   MADLKLTGVEKAYGEVRVLRDIDLTIEKGELIVFVGPSGCGKSTLLRMIAGLERITGGTL 60

Query: 61  ELDGRDITEVSPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVNKAEVEKKVNEAARI 120
           E+DG+ + +V PA+R +AMVFQ+YALYPHM+VR+NM FAL +AG +KAE+ + V  AARI
Sbjct: 61  EIDGQVVNDVPPAQRGIAMVFQSYALYPHMTVRQNMEFALKIAGQSKAEIARAVENAARI 120

Query: 121 LELGPMLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELARLH 180
           L+L P L+R P+ LSGGQRQRVAIGRAIVR+PK++LFDEPLSNLDAALRV  R+E+A+L 
Sbjct: 121 LQLTPYLDRLPRALSGGQRQRVAIGRAIVRDPKVYLFDEPLSNLDAALRVATRIEIAQLK 180

Query: 181 KEL-QATMIYVTHDQVEAMTLADKVVVLNGGRIEQVGSPLELYHQPANLFVAGFLGTPKM 239
           +++   TMIYVTHDQVEAMTLA ++VVL GG I QVG+PLELY +P N FVA F+G+P M
Sbjct: 181 EKMPDRTMIYVTHDQVEAMTLASRIVVLEGGGISQVGTPLELYTRPRNAFVARFIGSPAM 240

Query: 240 GFLKGKVTRVERQNCEVLLDAG--TRITLPLSGANLSIGGAVTLGIRPEHLNLALPGDCT 297
             L G++     +   V LD+G   R  +P    +L  G  V LG+RPE L +   G   
Sbjct: 241 NLLPGEIVETGPETV-VRLDSGGVARTAIPTEPEDL--GLLVDLGVRPEDL-VKTDGPPL 296

Query: 298 LQVTADVSERLGSDTFCH-VLTASGEALTMRIRGDLASRYGEQLSLHLDAEHCHLF 352
            +   +++E LG  T  + V    G  +  ++ G  A      + L  D    HLF
Sbjct: 297 YEGEVEITEALGEVTLLYFVPRDEGGQVVAKLPGIQADLRHRTVRLGADPARLHLF 352


Lambda     K      H
   0.321    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: 384
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: 367
Length of database: 369
Length adjustment: 30
Effective length of query: 337
Effective length of database: 339
Effective search space:   114243
Effective search space used:   114243
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 Apr 10 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