GapMind for catabolism of small carbon sources

 

Alignments for a candidate for put1 in Clostridium kluyveri DSM 555

Align proline dehydrogenase (EC 1.5.5.2) (characterized)
to candidate WP_012102398.1 CKL_RS10110 FAD-dependent oxidoreductase

Query= BRENDA::Q76M76
         (483 letters)



>NCBI__GCF_000016505.1:WP_012102398.1
          Length = 415

 Score =  308 bits (789), Expect = 2e-88
 Identities = 163/362 (45%), Positives = 242/362 (66%), Gaps = 9/362 (2%)

Query: 120 DVVVIGGGPAGLMAAIHAADAGASVILIDENPMLGGQLVKQTHKFFGKREQFAGVRGVKI 179
           D+V++G GPAGL A I A+ AGA V+++D N   GGQL KQ HKFFG     +GVRG+ I
Sbjct: 45  DIVIVGAGPAGLAAGIEASLAGAEVLMVDLNMKPGGQLFKQIHKFFGSSAHRSGVRGMDI 104

Query: 180 AEILGEEVKKRGNIEVFLETSAVGVF---HEGEEKLVAAVRKNKELLEFLGKTLVVATGA 236
              L ++ ++ G +E++L ++ +G+F     G EK      + ++L+    K +++A GA
Sbjct: 105 GRELVKKAEENG-VEIWLGSTVIGLFPGNKVGIEK--GNDNEKRKLITVKAKKIIIAAGA 161

Query: 237 MEKMIPFENNDLPGIYGAGAIQTLMNTYGVKPGDRVLIVGAGNVGLILAYQLIQAGVEVK 296
            E ++ F+    PG+ GAGA QT++N   VKPG++V+++G+GNVGLI++YQL+QAG EV 
Sbjct: 162 SENVVRFKGWTKPGVMGAGAAQTMVNVNHVKPGEKVVMLGSGNVGLIVSYQLMQAGCEVV 221

Query: 297 AIVEAMPKVGGYFVHAAKVRRLGVPILTRHTILRAEGKDRVERAVIAQLDENWRPVPGTE 356
           A+VEA PK+GGY VHAAK++R GVPI  RHTI+  +G ++V   VIA++DE +RP+ GTE
Sbjct: 222 ALVEAAPKIGGYGVHAAKIKRAGVPIYIRHTIIEVKGDNKVCEVVIAEVDEKYRPIVGTE 281

Query: 357 KVFEVDTIALAVGLRPSIELLHQAGCQVKFVRELSGHVAVRDGRMETTVQGIFVAGDSAG 416
           K+ + D +A+ VGL+PS+EL     CQ  F     G V + +  MET+ +GI+VAGD+ G
Sbjct: 282 KIIKADVVAIGVGLKPSVELARLLKCQFTFNALFGGEVPLHNKDMETSNEGIYVAGDTTG 341

Query: 417 IEEATTAMLEGKIAGIAAALKAGAASPEWLAEIEKAQ--RDLLEFRSGPFGRHVLEGIKK 474
           +EEA TA+ EG+IAGI+AA K G    + +AE +K +  + L   R GPFG   L   ++
Sbjct: 342 VEEANTALEEGRIAGISAAQKLGYIDDD-IAENKKKEIWQRLKSLRLGPFGERRLRAKEQ 400

Query: 475 VL 476
           ++
Sbjct: 401 IM 402


Lambda     K      H
   0.319    0.138    0.397 

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: 579
Number of extensions: 31
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: 483
Length of database: 415
Length adjustment: 33
Effective length of query: 450
Effective length of database: 382
Effective search space:   171900
Effective search space used:   171900
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: 51 (24.3 bits)

This GapMind analysis is from Sep 24 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