GapMind for catabolism of small carbon sources

 

Alignments for a candidate for puuA in Sinorhizobium meliloti 1021

Align Gamma-glutamyl-putrescine synthetase (EC 6.3.1.11) (characterized)
to candidate SMc01594 SMc01594 hypothetical protein

Query= reanno::BFirm:BPHYT_RS23160
         (444 letters)



>FitnessBrowser__Smeli:SMc01594
          Length = 454

 Score =  174 bits (441), Expect = 5e-48
 Identities = 121/378 (32%), Positives = 178/378 (47%), Gaps = 22/378 (5%)

Query: 71  DMVCVPDASTIRMIPWAVDPTAQVIHDCVHFDG-TPVAISPRRVLRRVLELYKAKGWKPV 129
           D    PD ST+R IPW ++ TA V+ D +  D    V  SPR +L++ +   +A G+K  
Sbjct: 79  DYTMKPDLSTLRRIPW-LEGTALVLCDMLDHDTHAEVPHSPRAILKKQVARLEAMGFKAY 137

Query: 130 IAPELEFYLVDMNKDP-------DLPLQPPIGRTGRPETGRQAYSIEAVNEFDPLFEDIY 182
           +A ELEF+L D + D        DL L              + Y I    + + +   I 
Sbjct: 138 MASELEFFLFDQSYDDARLSGYRDLQLASGYN---------EDYHIFQTTKEEDVMRAIR 188

Query: 183 EYCEVQELEVDTLIHEVGAAQMEINFMHGDPLKLADSVFLFKRTVREAALRHKMYATFMA 242
              +   + V+    E  A Q EIN  + D L +AD   + K   +E A +     TF+A
Sbjct: 189 NGLQGAGIPVENSKGEASAGQEEINVRYADALTMADRHAIIKNGCKEIAWQRGKAITFLA 248

Query: 243 KPMEGEPGSAMHMHQSLVDEETGHNLFTGPDGK--PTSLFTSYIAGLQKYTPALMPIFAP 300
           K      GS+ H+HQSL  ++    LF   +G+   + L   Y+AG   +   +    AP
Sbjct: 249 KWNYSAAGSSSHIHQSLWSKDGETPLFFDKNGQYGMSELMRHYVAGQLAHASEVTYFLAP 308

Query: 301 YINSYRRLSRFMAAPINVAWGYDNRTVGFRIPHSGPAARRIENRIPGVDCNPYLAIAATL 360
           YINSY+R      AP    W  DNRT G+R+   G  A RIE R+ G D NPYLA AA +
Sbjct: 309 YINSYKRFMAGTFAPTKAIWSKDNRTAGYRLCGEGSKAIRIECRVGGSDLNPYLAFAALI 368

Query: 361 AAGYLGMTQKLEATEPLLSDGYE--LPYQLPRNLEEGLTLMGACEPIAEVLGEKFVKAYL 418
           AAG  G+  K+E   P + D Y+     ++P  L E    +   + +    GE+ V  Y+
Sbjct: 369 AAGIAGIENKMELEAPFVGDAYQGKEVREIPHTLREAGEALSGSKMLRAAFGEEVVDHYV 428

Query: 419 ALKETEYEAFFRVISSWE 436
              E E + + R ++ WE
Sbjct: 429 HAAEWEQQEYDRRVTDWE 446


Lambda     K      H
   0.321    0.138    0.418 

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: 482
Number of extensions: 21
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: 444
Length of database: 454
Length adjustment: 33
Effective length of query: 411
Effective length of database: 421
Effective search space:   173031
Effective search space used:   173031
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 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