Align aspartate ammonia-lyase (EC 4.3.1.1) (characterized)
to candidate WP_092487237.1 BM299_RS16975 aspartate ammonia-lyase
Query= BRENDA::Q9LCC6 (468 letters) >NCBI__GCF_900115975.1:WP_092487237.1 Length = 482 Score = 453 bits (1166), Expect = e-132 Identities = 229/466 (49%), Positives = 316/466 (67%) Query: 3 TDVRIEKDFLGEKEIPKDAYYGVQTIRATENFPITGYRIHPELIKSLGIVKKSAALANME 62 T+ R+EKD LGE +P AYYGV T+RA +NF ++G R+HPEL+++L VK +AA AN + Sbjct: 2 TEHRMEKDLLGELPVPAQAYYGVHTLRAAQNFAVSGCRVHPELLRALAEVKWAAARANRQ 61 Query: 63 VGLLDKEVGQYIVKAADEVIEGKWNDQFIVDPIQGGAGTSINMNANEVIANRALELMGEE 122 GLL + + AA EV G+ DQFIVD +QGGAGTS NMN NEV+ANRA+EL+G + Sbjct: 62 AGLLTANIADAVSAAAREVARGQLADQFIVDALQGGAGTSTNMNMNEVLANRAIELLGGQ 121 Query: 123 KGNYSKISPNSHVNMSQSTNDAFPTATHIAVLSLLNQLIETTKYMQQEFMKKADEFAGVI 182 KG+Y + P +HVNMSQSTND +PTA IA + L+ L + +Q +K +FAGV+ Sbjct: 122 KGDYRLVHPLNHVNMSQSTNDTYPTALRIAAIRLVLALSDAMARLQGALQEKEAQFAGVL 181 Query: 183 KMGRTHLQDAVPILLGQEFEAYARVIARDIERIANTRNNLYDINMGATAVGTGLNADPEY 242 K+GRT LQDA+P+ LGQEF AYA +ARD R+ L IN+G TAVGTGLNA Y Sbjct: 182 KLGRTELQDALPVTLGQEFGAYAEAVARDRWRLYKVEERLRQINLGGTAVGTGLNAPRRY 241 Query: 243 ISIVTEHLAKFSGHPLRSAQHLVDATQNTDCYTEVSSALKVCMINMSKIANDLRLMASGP 302 I V E L + +G L A++ VD TQN D + EVS +K +N++KIA DL L+A+GP Sbjct: 242 IYQVVEELRQITGLGLARAENPVDLTQNADVFAEVSGLVKAAAVNLAKIAGDLMLLAAGP 301 Query: 303 RAGLSEIVLPARQPGSSIMPGKVNPVMPEVMNQVAFQVFGNDLTITSASEAGQFELNVME 362 GL+EI LP RQ GSSIMPGKVNPV+PE++ Q A+QV G D I A G+ ELN Sbjct: 302 AGGLAEINLPPRQAGSSIMPGKVNPVIPEMVTQAAWQVMGADQVICQACAGGRLELNAFL 361 Query: 363 PVLFFNLIQSISIMTNVFKSFTENCLKGIKANEERMKEYVEKSIGIITAINPHVGYETAA 422 P++ NL+ + I+ + F + C++GI ANE+R + ++E+S ++TA+ P++GYE AA Sbjct: 362 PLVAHNLLHGLEILAKTAQIFADKCVRGITANEQRCRRWLEESHVLVTALAPYIGYEQAA 421 Query: 423 KLAREAYLTGESIRELCIKYGVLTEEQLNEILNPYEMTHPGIAGRK 468 LAR A ++I+E+ ++ G+L+EE+ + + P E+T PGIAG + Sbjct: 422 ALARRAREQHKTIKEIVLESGLLSEEEWHALAAPRELTRPGIAGAR 467 Lambda K H 0.316 0.133 0.370 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: 555 Number of extensions: 20 Number of successful extensions: 1 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: 468 Length of database: 482 Length adjustment: 33 Effective length of query: 435 Effective length of database: 449 Effective search space: 195315 Effective search space used: 195315 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 (21.6 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Apr 09 2024. 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