Aligments for a candidate for edd in Synechococcus elongatus PCC 7942

GapMind for catabolism of small carbon sources

Aligments for a candidate for edd in Synechococcus elongatus PCC 7942

Align phosphogluconate dehydratase (EC 4.2.1.12) (characterized)
to candidate Synpcc7942_0626 Synpcc7942_0626 dihydroxy-acid dehydratase

Query= BRENDA::Q1PAG1
         (608 letters)



>lcl|FitnessBrowser__SynE:Synpcc7942_0626 Synpcc7942_0626
           dihydroxy-acid dehydratase
          Length = 619

 Score =  214 bits (546), Expect = 7e-60
 Identities = 173/558 (31%), Positives = 266/558 (47%), Gaps = 53/558 (9%)

Query: 68  VAIVSSYNDMLSAHQPYEHFPEQIKKALREMGSVGQFAGGTPAMCDGVTQGEAGMELSLP 127
           +A+ +S+   +  H   +   + + + +   G V +    T A+ DG+  G  GM  SLP
Sbjct: 37  IAVANSFTQFVPGHVHLKDLGQLVAREIERAGGVAK-EFNTIAVDDGIAMGHGGMLYSLP 95

Query: 128 SREVIALSTAVALSHNMFDAALMLGICDKIVPGLMMGALRFGHLPTIFVPGGPMPSG--I 185
           SR++IA S    ++ +  DA + +  CDKI PG++M ALR  ++P +FV GGPM +G  I
Sbjct: 96  SRDLIADSVEYMVNAHCADALVCISNCDKITPGMLMAALRL-NIPAVFVSGGPMEAGKVI 154

Query: 186 SNKEK-----ADVRQRYAEGKATREELLESEMKSYHSPGTCTFYGTANTNQLLMEVMGLH 240
            N E+      D     A+ + + E++   E  +  + G+C+   TAN+   L E +GL 
Sbjct: 155 LNGEERHLDLVDAMVVAADDRESDEDVATIERSACPTCGSCSGMFTANSMNCLTEALGLS 214

Query: 241 LPGASFVNPYTPLRDALTHEAAQQVTRLTKQSGNFTPIGEIVDERSLV------NSIVAL 294
           LPG   +      R  L  EA +   +L KQ   +    E V  RS+       N+I   
Sbjct: 215 LPGNGSLLATHGDRKELFLEAGRLAVKLAKQ--YYEQDDESVLPRSIASFKAFENAICLD 272

Query: 295 HATGGSTNHTLHMPAIAQAAGIQLTWQDMADLSEVVPTLSHVYPN-GKADINHFQAAGGM 353
            A GGSTN  LH+ A A  AG+  T +D+  LS  +P L  V P+  K  +     AGG+
Sbjct: 273 IAMGGSTNTVLHLLAAAHEAGVDFTMKDIDRLSRKIPNLCKVAPSTQKYHMEDVHRAGGV 332

Query: 354 AFLIRELLEAGLLHEDVNTVAGRGL-------------------SRY--------TQEPF 386
             ++ EL  AGLLH +V TV    L                   SRY        TQE F
Sbjct: 333 IAILGELDRAGLLHREVPTVHSPSLGAALDQWDINRETATEEAKSRYLAAPGGVPTQEAF 392

Query: 387 LDNGKLVWRDGPIESLDENILRPVARAFSPEGGLRVMEGNLGRG--VMKVSAVALQHQIV 444
             + +  W    ++  +   +R +  A+S +GGL V+ GNL     ++K + V     + 
Sbjct: 393 SQSKR--WTALDLDR-ENGCIRDIEHAYSQDGGLAVLYGNLAEQGCIVKTAGVDENILVF 449

Query: 445 EAPAVVFQDQQDLADAFKAGELEKDFVAVMRFQGPRSN-GMPELHKMTPFLGVLQDRGFK 503
             PAVV + Q +  +    G +++  V ++R++GPR   GM E+   T +L   +  G  
Sbjct: 450 SGPAVVCESQDEAVNWILNGRVKEGDVVLIRYEGPRGGPGMQEMLYPTSYL-KSKGLGKA 508

Query: 504 VALVTDGRMSGASGKIPAAIHVSPEAQVGGALARVRDGDIIRVDGVKGTLELKVDADEFA 563
            AL+TDGR SG +  +    HVSPEA  GG +A V  GD I +D     + L V  +E A
Sbjct: 509 CALITDGRFSGGTSGLSIG-HVSPEAAEGGLIALVEQGDRIEIDIPNRRIHLAVSEEELA 567

Query: 564 AREPAKGLLGNNVGSGRE 581
            R  A    G+   + ++
Sbjct: 568 HRRAAMEARGDQAWTPKD 585


Lambda     K      H
   0.318    0.134    0.386 

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: 924
Number of extensions: 50
Number of successful extensions: 9
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: 608
Length of database: 619
Length adjustment: 37
Effective length of query: 571
Effective length of database: 582
Effective search space:   332322
Effective search space used:   332322
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 preprint 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