GapMind for catabolism of small carbon sources

 

Alignments for a candidate for citrullinase in Pedobacter sp. GW460-11-11-14-LB5

Align arginine deiminase (EC 3.5.3.6) (characterized)
to candidate CA265_RS10475 CA265_RS10475 amidinotransferase

Query= reanno::pseudo3_N2E3:AO353_25635
         (311 letters)



>FitnessBrowser__Pedo557:CA265_RS10475
          Length = 304

 Score =  300 bits (768), Expect = 3e-86
 Identities = 155/305 (50%), Positives = 208/305 (68%), Gaps = 1/305 (0%)

Query: 1   MQTTNTVLMIRPTRFSFNQDTAANNRFQRPAAAAEDVQLKALQEFDGYVAALREHGVEVM 60
           MQTTN +LMIRP  F FN+ TA NN+FQ  A+   +VQ +AL+EFD +V  LR++ V+V 
Sbjct: 1   MQTTNHILMIRPVDFKFNEQTAGNNKFQ-VASTETNVQTEALKEFDAFVDLLRKNNVDVT 59

Query: 61  VHNDSEAPHTPDSIFPNNWWSSHPDGTLVLYPMQGHNRRLERDKGVLDWLRDAYRIEQLL 120
           V +D+  P TPDSIFPNNW S H DG++ LYPM   NRRLER K +LD L++ + +  + 
Sbjct: 60  VVDDTLQPETPDSIFPNNWVSFHEDGSVYLYPMFSENRRLERRKEILDGLKENFEVNHIS 119

Query: 121 DLSDLEQQEVFLEGTGSMVLDREQRICYAGYSTRTHAKALDQVVEHLGYELCAFNAVDRH 180
           DLS  E Q  FLEGTGSMVLDR  +I YA  S RT  + LD      GYE  AF AVD  
Sbjct: 120 DLSFYEHQHAFLEGTGSMVLDRTNKIAYACLSVRTDEEVLDNFCMLTGYEPVAFQAVDES 179

Query: 181 GVPIYHTNVMMSVGRQLAVVCLESVSDLDERNALRSRLECSGKQVLTLSFDQLESFAGNM 240
             PIYHTNVMM +G + AV+CL+S+ D +E+  +   L+ SGK+++ ++ +Q+  FAGNM
Sbjct: 180 NFPIYHTNVMMCIGDRFAVICLDSIKDPEEKLNVTISLKGSGKEIIEINLEQMNKFAGNM 239

Query: 241 LEVHNAAGEPLLVMSRTAWRSLHADQRRMVEAYAKPLPVNIDTIERIGGGSARCMLAEVY 300
           L++ NA  E LLVMS  A+ SL A+Q   +E Y++ +   + TIE+ GGGSARCMLAE++
Sbjct: 240 LQLTNADDESLLVMSEQAYLSLTAEQIVALEQYSRIIYAPLYTIEKNGGGSARCMLAEIH 299

Query: 301 LPKRV 305
           LP ++
Sbjct: 300 LPSKL 304


Lambda     K      H
   0.320    0.133    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: 239
Number of extensions: 8
Number of successful extensions: 2
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: 311
Length of database: 304
Length adjustment: 27
Effective length of query: 284
Effective length of database: 277
Effective search space:    78668
Effective search space used:    78668
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: 48 (23.1 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