GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ltaE in Sphingomonas koreensis DSMZ 15582

Align L-threonine aldolase (EC 4.1.2.5) (characterized)
to candidate Ga0059261_2028 Ga0059261_2028 L-threonine aldolase (EC 4.1.2.5)

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1114
         (346 letters)



>FitnessBrowser__Korea:Ga0059261_2028
          Length = 333

 Score =  273 bits (698), Expect = 5e-78
 Identities = 154/335 (45%), Positives = 202/335 (60%), Gaps = 7/335 (2%)

Query: 7   QFASDNYSGICPEAWAAMEQANHGHQRAYGDDEWTARASDGFRKLFETDCEVFFAFNGTA 66
           +F SDN +  CPE  AA+  AN     AY  D  +      F +LFETD  V +   GTA
Sbjct: 2   RFFSDNAAPACPEVLAALTAANV-QDTAYDGDALSQSLDARFSELFETDAAVLWLPTGTA 60

Query: 67  ANSLALSSLCQSYHSVICSETAHVETDECGAPEFFSNGSKLLIARTENGKLTPDSIREVA 126
           AN LAL+SLC  Y  V+C   AH++ DE GAPEFF++G+KLL+A     KLTPD+IR V 
Sbjct: 61  ANCLALASLCPPYGGVVCHREAHIQADEAGAPEFFTHGAKLLLAEGAGAKLTPDAIRAVI 120

Query: 127 LK-RQDIHYPKPRVVTLTQATEVGSVYTPDEIRAISATCKELGLNLHMDGARFSNACAFL 185
            + +  +H+ +P  +++T ATE G  YTP E  AI A  KE GL  H+DGARF+NA   L
Sbjct: 121 DRIKPGVHWTQPHAISITNATEYGLAYTPQETAAIGALAKERGLGFHVDGARFANALVHL 180

Query: 186 GCTPADLTWKAGVDVLCFGGTKNGMAVGEAILFFNHKLAEDFDYRCKQAGQLASKMRFLS 245
           GCTPADL+W+AGVD L FG  KNG    EA++FF   LA+    R K+AG L SK RFL+
Sbjct: 181 GCTPADLSWRAGVDALSFGFIKNGGMGAEALVFFRPDLAQAARVRRKRAGHLQSKGRFLA 240

Query: 246 APWVGILENDAWLKYANHANHCAQLLAELVSDIPGVELMFPVQANGVFLQLSEPAIAALT 305
           A    +L+ + WL+ A  AN  A LLA+      G  L+ PVQ+N +FL+ +    A+L 
Sbjct: 241 AQLHAMLDGELWLRNARAANAGAALLAQAA----GPRLLHPVQSNALFLKATAEEAASLR 296

Query: 306 AKGWRFYTFIGNGGARFMCSWDTEQERVRELAKDI 340
           A+G+ FY +   G  R + SWD +   VR LA  I
Sbjct: 297 AQGFGFYDW-APGEIRVVVSWDQDAAAVRPLADAI 330


Lambda     K      H
   0.320    0.133    0.416 

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: 287
Number of extensions: 14
Number of successful extensions: 4
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: 346
Length of database: 333
Length adjustment: 28
Effective length of query: 318
Effective length of database: 305
Effective search space:    96990
Effective search space used:    96990
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 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