Align Probable 2-ketoarginine decarboxylase AruI; 2-oxo-5-guanidinopentanoate decarboxylase; 5-guanidino-2-oxopentanoate decarboxylase; EC 4.1.1.75 (characterized)
to candidate WP_055434897.1 ASC41_RS01605 biosynthetic-type acetolactate synthase large subunit
Query= SwissProt::Q9HUI8 (559 letters) >NCBI__GCF_001418085.1:WP_055434897.1 Length = 577 Score = 203 bits (516), Expect = 2e-56 Identities = 161/515 (31%), Positives = 243/515 (47%), Gaps = 23/515 (4%) Query: 25 QPQKTLTAGQALVRLLANYGVDTVFGIPGVHTLELYRGLPG--SGIRHVLTRHEQGAGFM 82 Q + ++ +A++R L GVD ++G PG + +Y L I HVLTRHEQGA Sbjct: 14 QTTERISGSEAVIRCLLAEGVDILYGYPGGAIMPVYDELYKYQDKIHHVLTRHEQGATHS 73 Query: 83 ADGYARVSGKPGVCFVITGPGVTNVATAIGQAYADSVPLLVISSVNHSASLGKGWGCLHE 142 A GYAR+SGK GV +GPG TN+ T I A DS P++ I+ S LG E Sbjct: 74 AQGYARISGKVGVAIATSGPGATNLITGIADAQIDSTPMVCITGQVASHLLGS--DAFQE 131 Query: 143 TQDQRAMTAPITAFSALALSPEQLPELIARAYAVFDSERPRPVHISIPLDVLAAPVAHDW 202 T D ++ P+T ++ Q+PE +A+A+ + S RP PV I I D + Sbjct: 132 T-DIVGISTPVTKWNCQVTKASQIPEAMAKAFYIARSGRPGPVLIDITKDAQFEEFDFKY 190 Query: 203 SAAVARRPGRGVPCSE--ALRAAAERLAAARRPMLIAGGGALAAGEALA---ALSERLAA 257 R +P + ++ AAA+ + AA++PM++ G G + GEA A A+ E+ Sbjct: 191 EKCKGVRSYIPIPKLDQTSVEAAAKLINAAKKPMIVWGQGVI-LGEAEAEFKAVVEKAGI 249 Query: 258 PLFTSVAGKGLLPPDAPLN---AGASLCVAPGWEMIAEADLVLAVGTEMAD-TDFWRERL 313 P ++ G G +P PLN G AP + + D+++A+G D Sbjct: 250 PSAWTILGAGAIPTSHPLNIGMVGMHGNYAPN-VLTNDCDVLIAIGMRFDDRVTGSLSTY 308 Query: 314 PLSGELIRVDIDPRKFNDFYPSAVALRGDARQTLEALLVRLPQ----EARDSAPAAARVA 369 ++I DIDP + + + VA+ GD++++L ALL L + E + Sbjct: 309 AKQAKVIHFDIDPAEIDKNVKTDVAVLGDSKESLAALLPLLEEKTYPEWHQKFKDLYAIE 368 Query: 370 RLRAEIRAAHAPLQALHQA-ILDRIAAALPADAFVSTDMTQLAYTGNYAFASRAPRSWLH 428 + H + L A +L I DA + TD+ Q RS + Sbjct: 369 YEKVIKHDLHPTKEGLTMAEVLKEINIQTKGDAAIVTDVGQHQMIACRYANFNKTRSNIT 428 Query: 429 PTGYGTLGYGLPAGIGAKLGAPQRPGLVLVGDGGFLYTAQELATASEELDSPLVVLLWNN 488 G GT+G+GLPA IGAK+ AP R + + GDGG+ T QEL T ++ +V+L NN Sbjct: 429 SGGLGTMGFGLPAAIGAKMAAPDREVISISGDGGYQMTIQELGTIFQQKAGVKIVVL-NN 487 Query: 489 DALGQIRD-DMLGLDIEPVGVLPRNPDFALLGRAY 522 + LG +R + D NPDF + + Y Sbjct: 488 EFLGMVRQWQEMFFDRRYASTEMTNPDFVAIAKGY 522 Lambda K H 0.321 0.136 0.412 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: 674 Number of extensions: 43 Number of successful extensions: 6 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: 559 Length of database: 577 Length adjustment: 36 Effective length of query: 523 Effective length of database: 541 Effective search space: 282943 Effective search space used: 282943 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: 53 (25.0 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
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:
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