Alignments for a candidate for dgoD in Sinorhizobium meliloti 1021

GapMind for catabolism of small carbon sources

Alignments for a candidate for dgoD in Sinorhizobium meliloti 1021

Align L-arabinonate dehydratase; ArDHT; D-fuconate dehydratase; Galactonate dehydratase; L-arabonate dehydratase; EC 4.2.1.25; EC 4.2.1.67; EC 4.2.1.6 (characterized)
to candidate SM_b20115 SM_b20115 dihydroxy-acid dehydratase

Query= SwissProt::B5ZZ34
         (579 letters)



>FitnessBrowser__Smeli:SM_b20115
          Length = 573

 Score =  519 bits (1337), Expect = e-151
 Identities = 260/567 (45%), Positives = 371/567 (65%), Gaps = 3/567 (0%)

Query: 11  LRSQEWYGGTSRDVIYHRGWLKNQGYPHDLFDGRPVIGILNTWSDMTPCNGHLRELAEKV 70
           LRS  W+         HR  L   GY    +  +P+I ILNTWSD+ PC+ H +   + V
Sbjct: 5   LRSARWFAPDDLRSSGHRSRLMQMGYDAKDWGEKPIIAILNTWSDLNPCHAHFKHRIDDV 64

Query: 71  KAGVWEAGGFPLEVPVFSASENTFRPTAMMYRNLAALAVEEAIRGQPMDGCVLLVGCDKT 130
           K GV +AGGFP+E+PV S SE++ +PT M+YRN  A+  EE +RG P+DG VL+ GCDKT
Sbjct: 65  KRGVLQAGGFPVELPVQSLSESSLKPTTMLYRNFLAMEAEELLRGHPIDGAVLMGGCDKT 124

Query: 131 TPSLLMGAASCDLPSIVVTGGPMLNGYFRGERVGSGTHLWKFSEMVKAGEMTQAEFLEAE 190
           TP+L+MGA S  LP I +  GPML G+++GE +GSG+  WK+ +  +AG +T  +++  E
Sbjct: 125 TPALVMGAISAGLPMIFLPSGPMLRGHYKGEHLGSGSDAWKYWDERRAGTITDEQWIGVE 184

Query: 191 ASMSRSSGTCNTMGTASTMASMAEALGMALSGNAAIPGVDSRRKVMAQLTGRRIVQMVKD 250
             ++RS G C T GTASTM ++AE+LG+ L G ++IP  D+    M+   GRRIV+MV +
Sbjct: 185 EGIARSYGHCMTFGTASTMTAIAESLGLTLPGASSIPAADANHIRMSTRCGRRIVEMVHE 244

Query: 251 DLKPSEIMTKQAFENAIRTNAAIGGSTNAVIHLLAIAGRVGIDLSLDDWDRCGRDVPTIV 310
            L P +I+T+++  NA     A G STNAV+HL+A+A R G+ L+L+D D   R  P I 
Sbjct: 245 KLGPEKIITEKSVANASAVAMATGCSTNAVVHLIAMARRAGVPLTLEDLDGISRTTPVIA 304

Query: 311 NLMPSGK-YLMEEFFYAGGLPVVLKRLGEAGLLHKDALTVSGETVWDEVKDVVNWNEDVI 369
           N+ PSGK YLME+F+YAGGL  ++  + E  LLH DA+TVSG  +   ++     N DVI
Sbjct: 305 NIRPSGKQYLMEDFYYAGGLRALMAEMKE--LLHLDAMTVSGFPLGATLEGAEVHNSDVI 362

Query: 370 LPAEKALTSSGGIVVLRGNLAPKGAVLKPSAASPHLLVHKGRAVVFEDIDDYKAKINDDN 429
            P    +   G + VL+GNLAP G V+KPSA    L VH+G A+VF+   + KA I+D++
Sbjct: 363 RPLSNPIYHEGSLAVLKGNLAPDGCVVKPSACEERLRVHEGPALVFDSYPEMKAAIDDED 422

Query: 430 LDIDENCIMVMKNCGPKGYPGMAEVGNMGLPPKVLKKGILDMVRISDARMSGTAYGTVVL 489
           LD+  + +++++N GPKG PGM E G + +P K+LK+G  DM+RISDARMSGT+YG  +L
Sbjct: 423 LDVTPDHVLILRNAGPKGGPGMPEWGMLPIPKKILKQGYRDMLRISDARMSGTSYGACIL 482

Query: 490 HTSPEAAVGGPLAVVKNGDMIELDVPNRRLHLDISDEELARRLAEWQPNHDLPTSGYAFL 549
           H +PE+ VGGPL++V+ GD+I +DV NR + + + +E LA R A W    D    GY ++
Sbjct: 483 HVAPESHVGGPLSLVRTGDIIRVDVANRTIDMLVDEEILAMRRAAWTRPADKYERGYGWM 542

Query: 550 HQQHVEGADTGADLDFLKGCRGNAVGK 576
             +H++ A+ G D DFL+   G AVG+
Sbjct: 543 FSKHIKQANEGCDFDFLETAFGTAVGE 569


Lambda     K      H
   0.318    0.135    0.408 

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: 1010
Number of extensions: 43
Number of successful extensions: 3
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: 579
Length of database: 573
Length adjustment: 36
Effective length of query: 543
Effective length of database: 537
Effective search space:   291591
Effective search space used:   291591
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 53 (25.0 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
Organisms (tab-delimited)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources