Aligments for a candidate for edd in Phaeobacter inhibens BS107

GapMind for catabolism of small carbon sources

Aligments for a candidate for edd in Phaeobacter inhibens BS107

Align phosphogluconate dehydratase (characterized)
to candidate GFF2902 PGA1_c29490 dihydroxy-acid dehydratase LivD

Query= CharProtDB::CH_024239
         (603 letters)



>lcl|FitnessBrowser__Phaeo:GFF2902 PGA1_c29490 dihydroxy-acid
           dehydratase LivD
          Length = 614

 Score =  182 bits (463), Expect = 3e-50
 Identities = 156/538 (28%), Positives = 251/538 (46%), Gaps = 45/538 (8%)

Query: 68  IAIITSYNDMLSAHQPYEHYPEIIRKALHEANAVGQVAGGVPAMCDGVTQGQDGMELSLL 127
           IAI+ S+   +  H   +   +++ + +  A  V +    + A+ DG+  G DGM  SL 
Sbjct: 37  IAIVNSFTQFVPGHVHLKDLGQMVAREVEAAGGVAKEFNTI-AVDDGIAMGHDGMLYSLP 95

Query: 128 SREVIAMSAAVGLSHNMFDGALFLGVCDKIVPGLTMAALSFGHLPAVFVPSGPMASGL-- 185
           SREVIA S    ++ +  D  + +  CDKI PG+ MAA+   ++PA+FV  GPM +G   
Sbjct: 96  SREVIADSVEYMVNAHCADAMVCISNCDKITPGMLMAAMRL-NIPAIFVSGGPMEAGKID 154

Query: 186 ---PNKEKVRIRQLYAEGKVDRMA---LLESEAASYHAPGTCTFYGTANTNQMVVEFMGM 239
               + +K+ +         D M    +   E  +    G+C+   TAN+   + E +G+
Sbjct: 155 IADLDMKKIDLVDAMVAAASDTMTDEQVQHIEENACPTCGSCSGMFTANSMNCLAEALGL 214

Query: 240 QLPGSSFVHPDSPLRDALTAAAARQVTRMTGN---GNEWMPIGKMIDEKVVVNGIVAL-L 295
            LPG+         R  L   A R++  +T     G E   + + I         ++L +
Sbjct: 215 ALPGNGSTLATHADRKHLFLEAGRKIVDITKRHYVGEEKGLLPREIATFDAFENAMSLDI 274

Query: 296 ATGGSTNHTMHLVAMARAAGIQINWDDFSDLSDVVPLMARLYPN-GPADINHFQAAGGVP 354
           A GGSTN  +HL+A+A    +     D   LS  VP + ++ PN     +     AGG+ 
Sbjct: 275 AMGGSTNTVLHLLAIANEGKVDFTMTDMDRLSRKVPCLCKVAPNIENVHMEDVHRAGGIF 334

Query: 355 VLVRELLKAGLLHEDVNTV----AGFGLSRYTLEPWLN---------------NGELDWR 395
            ++ EL +AGLLH + +TV     G  ++++ ++   N                 E   +
Sbjct: 335 SILGELSRAGLLHNECSTVHSSTMGEAIAKWDIKVANNPDAEALFKAAPGGVRTTEAFSQ 394

Query: 396 EGAEKSLDSN----VIASFEQPFSHHGGTKVLSGNLGR--AVMKTSAVPVENQVIEAPAV 449
               K LD++    VI S +  FS  GG  VL GN+ R   ++KT+ V          A 
Sbjct: 395 SNRYKELDTDREGGVIRSKDHAFSQDGGLAVLFGNIARDGCIVKTAGVDDNILKFTGSAY 454

Query: 450 VFESQHDVMPAFEAGLLDRDCVVVVRHQGPKANGMPELHKLMPPLGVLLDRCF--KIALV 507
           V ESQ   +       +    VVV+R++GP+  G P + +++ P   L  +      AL+
Sbjct: 455 VCESQDQAVNDILTSKVKEGDVVVIRYEGPR--GGPGMQEMLYPTSYLKSKGLGKACALL 512

Query: 508 TDGRLSGASGKVPSAIHVTPEAYDGGLLAKVRDGDIIRVNGQTGELTLLVDEAELAAR 565
           TDGR SG +  + S  HV+PEA +GG +  V+ GD I ++     + L V + ELAAR
Sbjct: 513 TDGRFSGGTSGL-SIGHVSPEAAEGGTIGLVQQGDTIEIDIPNRTIHLAVSDEELAAR 569


Lambda     K      H
   0.318    0.134    0.392 

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: 877
Number of extensions: 53
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: 603
Length of database: 614
Length adjustment: 37
Effective length of query: 566
Effective length of database: 577
Effective search space:   326582
Effective search space used:   326582
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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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