Align N-succinylornithine carbamoyltransferase (EC 2.1.3.11) (characterized)
to candidate PP_1079 PP_1079 Ornithine carbamoyltransferase
Query= reanno::Cola:Echvi_3849 (313 letters) >FitnessBrowser__Putida:PP_1079 Length = 306 Score = 103 bits (257), Expect = 5e-27 Identities = 87/287 (30%), Positives = 132/287 (45%), Gaps = 35/287 (12%) Query: 35 RGKRIGLLFLNPSLRTRVSTQIAASNLGMESIVLNMDKESWALEMEDGVIMNQGKAEHIR 94 + + +G++F S RTRVS + LG ++I L+ G+ E I Sbjct: 41 KNRVLGMIFEKSSTRTRVSFEAGMIQLGGQAIFLSPRDTQL------------GRGEPIG 88 Query: 95 DAAGVLGSYFDILALRAFPSLTNKDEDSEDFILHQFAKHSGLPLISLESAIRHPLQSLAD 154 D+A VL S D++ +R T L +FA S +P+I+ S HP Q LAD Sbjct: 89 DSAIVLSSMVDVVMIRTHAHST----------LTEFAAKSRVPVINGLSDESHPCQLLAD 138 Query: 155 MVTIQEHKQKEKPKVVLTWAPHIKAIPHAVANSFAEWSIGCGHDVTITHPEGYELDERFT 214 M T EH+ + K V TW + NS+ E + + I PEGYE D+RF Sbjct: 139 MQTFVEHRGSIQGKTV-TWIGD----GFNMCNSYIEAARQFDFQLRIACPEGYEPDQRFM 193 Query: 215 ----QGATIEHDQDKALANADFVYVKNWSAFN---EYGKILCTDESWMLNEQKLS-QAPN 266 I D +A+ +A V W++ E + L + + + L AP+ Sbjct: 194 ALGGDRVQIIRDAREAVRDAHLVVTDVWTSMGQEEETARRLAHFAPYQVTRELLDLAAPD 253 Query: 267 AKVMHCLPVRRNVELSDEILDGPRSLVQHQAKNRVFAAQAALSELLK 313 MHCLP R E+S ++LD PRS+ +A+NR+ A +A L L++ Sbjct: 254 VLFMHCLPAHRGEEISQDLLDDPRSVAWDEAENRLHAQKALLEFLVE 300 Lambda K H 0.317 0.132 0.384 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: 196 Number of extensions: 10 Number of successful extensions: 3 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: 313 Length of database: 306 Length adjustment: 27 Effective length of query: 286 Effective length of database: 279 Effective search space: 79794 Effective search space used: 79794 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: 48 (23.1 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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