GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Dyella japonica UNC79MFTsu3.2

Align D-glucosaminate dehydratase (EC 4.3.1.9) (characterized)
to candidate N515DRAFT_2222 N515DRAFT_2222 D-serine dehydratase

Query= reanno::pseudo5_N2C3_1:AO356_00450
         (405 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2222
          Length = 426

 Score =  371 bits (953), Expect = e-107
 Identities = 197/396 (49%), Positives = 263/396 (66%), Gaps = 9/396 (2%)

Query: 15  ATVGAHLLK-DVSLPALVLHRAALEHNIRWMQAFVTDSGAELAPHGKTSMTPALFRRQLD 73
           A+ G +LLK D+SLP  VL ++ LEHN+ WMQ F ++ GA LAPHGKT+M P LF RQL+
Sbjct: 35  ASHGWNLLKEDLSLPVAVLSQSRLEHNLAWMQRFASEYGARLAPHGKTTMAPRLFARQLE 94

Query: 74  AGAWGLTLATAVQTRAAYAHGVRRVLMANQLVGTPNMALIADLLADPAFEFHCMVDHPDN 133
           AGAWG+TLATA Q RAAY HGVRR+L+ANQLVG  NMA++A+LLADP+FEF C+VD  + 
Sbjct: 95  AGAWGITLATAQQARAAYVHGVRRILLANQLVGRRNMAIVAELLADPSFEFFCLVDAAEQ 154

Query: 134 VADLGAFFASRGMKLNVMIEYGVVGGRCGCRTEAEVLALAEAI-RSQPALALTGIEGYEG 192
           V  L AFF + G ++ V+IE GV GGR G R EA+  A+ +A+ +S  A++L G+E YEG
Sbjct: 155 VRQLAAFFGAAGRRIQVLIELGVPGGRTGVRDEAQWQAVLDALAQSGGAVSLAGVEVYEG 214

Query: 193 VIHGDHAISGIRAFAASLVRLAVQLQDDDAFAIDKPIITASGSAWYDLIAESFEAQNAHG 252
           V+  + A   IRAF    V     L  D        +++ +GSAWYD++AE F       
Sbjct: 215 VLKDETA---IRAFLQRGVEAVQVLARDGRLQRTPAVLSGAGSAWYDVVAEEFAKAQIGA 271

Query: 253 RFLSVLRPGSYVAHDHGIYKEAQCCV---LERRSDLHEGLRPALEVWAHVQSLPEPGFAV 309
               VLRPG Y+ HD G Y+ AQ  +     +   +   L PAL+VWA+VQS+PEP  A+
Sbjct: 272 PLDVVLRPGCYLTHDVGAYRIAQARIDASNPQARRMRSSLLPALQVWAYVQSVPEPECAI 331

Query: 310 IALGKRDVAYDAGLPVPLKRYTPGSDSVPGDDVSGCKVTAVMDQHAFMSVAAGVELRVGD 369
           +A+GKRD A+DAG P P   + PG  S P       +VT +MDQHA++ +AAG +LRVGD
Sbjct: 332 VAMGKRDAAFDAGFPSPAAHFRPGG-SAPSPVPPHWEVTGMMDQHAYLKIAAGDDLRVGD 390

Query: 370 IIAFGTSHPCLTFDKWRVGCLVDEQLRVVESMETCF 405
           ++AF  SHPCLTFDKWR   ++D+   VV+ ++T F
Sbjct: 391 MLAFDISHPCLTFDKWRQLPVIDDAYDVVDVVQTYF 426


Lambda     K      H
   0.322    0.136    0.414 

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: 525
Number of extensions: 24
Number of successful extensions: 5
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: 405
Length of database: 426
Length adjustment: 31
Effective length of query: 374
Effective length of database: 395
Effective search space:   147730
Effective search space used:   147730
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: 50 (23.9 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