GapMind for catabolism of small carbon sources

 

Alignments for a candidate for hutG in Mycolicibacterium vanbaalenii PYR-1

Align Formimidoylglutamase; Formiminoglutamase; Formiminoglutamate hydrolase; N-formimino-L-glutamate formiminohydrolase; EC 3.5.3.8 (characterized)
to candidate WP_036372852.1 MVAN_RS15185 agmatinase

Query= SwissProt::P42068
         (319 letters)



>NCBI__GCF_000015305.1:WP_036372852.1
          Length = 340

 Score =  157 bits (398), Expect = 3e-43
 Identities = 97/305 (31%), Positives = 155/305 (50%), Gaps = 10/305 (3%)

Query: 13  SFKDRDVTKMSDLIATWDGQDIKGPALIGVPLSKSSISHSGASFAPGTIRQALKHSSAYS 72
           SF  R     S+ + +W   D+   A++G P    + +  GA F P  IR        Y 
Sbjct: 14  SFGHRPFLTESEQLDSWK-PDV---AVVGAPFDVGTTNRPGARFGPRAIRATAYEPGTYH 69

Query: 73  AELGEHVVSEL-LYDLGDIDIHVTDIVKSHHHIFQTMHALLSDHPDWVPLILGGDNSISY 131
            +LG  +   L + D GD          SH +I + +HA+       VP+ILGGD+SI++
Sbjct: 70  MDLGLEIFDWLEVVDFGDAYCPHGQTEVSHRNIRERVHAVADR--GIVPVILGGDHSITW 127

Query: 132 STIKAIAQTKG--TTAVIQFDAHHDVRNTEDGG-PTNGTPFRRLLDEEIIEGQHLIQLGI 188
               A+A   G     ++ FDAH D  +  +G   ++GTP RRL++   + G H +Q+G+
Sbjct: 128 PAATAVADVHGYGNVGIVHFDAHADTADEIEGNLASHGTPMRRLIESGAVPGSHFVQVGL 187

Query: 189 REFSNSQAYEAYAKKHNVNIHTMDMIREKGLIPTIKEILPVVQDKTDFIFISVDMDVLDQ 248
           R +   Q    +  +  +  HTM  I E+G    + + +     K D +++SVD+DVLD 
Sbjct: 188 RGYWPPQDTFEWMLEQKMTWHTMQEIWERGFKAVMADAVAEALAKADKLYVSVDIDVLDP 247

Query: 249 SHAPGCPAIGPGGLYTDELLEAVKYIAQQPNVAGIEIVEVDPTLDFRDMTSRAAAHVLLH 308
           +HAPG     PGG+ + +LL  V+ +  + +V G+++VEV P  D  ++T  AA  V+  
Sbjct: 248 AHAPGTGTPEPGGITSADLLRMVRQLCHEHDVVGVDVVEVAPAYDHAELTINAAHRVVFE 307

Query: 309 ALKGM 313
           AL GM
Sbjct: 308 ALAGM 312


Lambda     K      H
   0.318    0.136    0.396 

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: 324
Number of extensions: 19
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: 319
Length of database: 340
Length adjustment: 28
Effective length of query: 291
Effective length of database: 312
Effective search space:    90792
Effective search space used:    90792
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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