Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7XAB8
PDB structure(s): 7am2_BT
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032543 | mitochondrial translation | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043043 | peptide biosynthetic process | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003924 | GTPase activity | 7 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 77 | 81 | PF00656 | 0.345 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.454 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.649 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 455 | 457 | PF00082 | 0.675 |
CLV_PCSK_PC7_1 | 193 | 199 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.554 |
DEG_APCC_DBOX_1 | 400 | 408 | PF00400 | 0.603 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.614 |
DEG_SCF_FBW7_1 | 205 | 212 | PF00400 | 0.478 |
DEG_SCF_FBW7_1 | 228 | 235 | PF00400 | 0.538 |
DEG_SPOP_SBC_1 | 352 | 356 | PF00917 | 0.598 |
DOC_CKS1_1 | 229 | 234 | PF01111 | 0.538 |
DOC_CYCLIN_yCln2_LP_2 | 407 | 413 | PF00134 | 0.741 |
DOC_MAPK_gen_1 | 197 | 207 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 160 | 169 | PF00069 | 0.383 |
DOC_PP1_RVXF_1 | 99 | 106 | PF00149 | 0.386 |
DOC_PP2B_LxvP_1 | 234 | 237 | PF13499 | 0.538 |
DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.407 |
DOC_SPAK_OSR1_1 | 325 | 329 | PF12202 | 0.506 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.579 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.745 |
LIG_14-3-3_CanoR_1 | 148 | 157 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 21 | 30 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 347 | 357 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 446 | 454 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 82 | 92 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 93 | 102 | PF00244 | 0.415 |
LIG_Actin_WH2_2 | 336 | 352 | PF00022 | 0.539 |
LIG_APCC_ABBAyCdc20_2 | 408 | 414 | PF00400 | 0.755 |
LIG_eIF4E_1 | 269 | 275 | PF01652 | 0.496 |
LIG_EVH1_1 | 154 | 158 | PF00568 | 0.561 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.405 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.474 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.538 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.425 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.510 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.703 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.591 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.573 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.722 |
LIG_GBD_Chelix_1 | 266 | 274 | PF00786 | 0.360 |
LIG_LIR_Gen_1 | 41 | 51 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 41 | 46 | PF02991 | 0.534 |
LIG_PCNA_yPIPBox_3 | 116 | 125 | PF02747 | 0.459 |
LIG_Pex14_2 | 11 | 15 | PF04695 | 0.504 |
LIG_Pex14_2 | 327 | 331 | PF04695 | 0.451 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.548 |
LIG_SH2_CRK | 229 | 233 | PF00017 | 0.451 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.354 |
LIG_SH2_NCK_1 | 229 | 233 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 271 | 275 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.660 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.486 |
LIG_SH3_2 | 155 | 160 | PF14604 | 0.555 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.488 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.216 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.515 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.395 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.669 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.494 |
LIG_SUMO_SIM_anti_2 | 340 | 345 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 203 | 208 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 223 | 231 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 73 | 80 | PF11976 | 0.356 |
LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.494 |
LIG_TYR_ITIM | 157 | 162 | PF00017 | 0.579 |
LIG_UBA3_1 | 153 | 160 | PF00899 | 0.570 |
LIG_WW_2 | 155 | 158 | PF00397 | 0.574 |
MOD_CDK_SPxxK_3 | 419 | 426 | PF00069 | 0.680 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.541 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.517 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.687 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.450 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.675 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.749 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.702 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.556 |
MOD_DYRK1A_RPxSP_1 | 198 | 202 | PF00069 | 0.477 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.459 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.578 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.489 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.456 |
MOD_GlcNHglycan | 305 | 309 | PF01048 | 0.442 |
MOD_GlcNHglycan | 31 | 35 | PF01048 | 0.572 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.557 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.516 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.488 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.445 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.467 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.448 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.400 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.571 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.463 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.588 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.578 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.674 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.409 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.452 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.452 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.482 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.559 |
MOD_PKA_1 | 455 | 461 | PF00069 | 0.686 |
MOD_PKA_1 | 93 | 99 | PF00069 | 0.553 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.671 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.414 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.513 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.643 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.576 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.418 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.490 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.627 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.445 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.627 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.465 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.447 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.450 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.639 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.733 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.747 |
MOD_SUMO_rev_2 | 41 | 51 | PF00179 | 0.606 |
TRG_DiLeu_BaLyEn_6 | 354 | 359 | PF01217 | 0.695 |
TRG_DiLeu_BaLyEn_6 | 98 | 103 | PF01217 | 0.406 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.346 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 417 | 420 | PF00400 | 0.718 |
TRG_NLS_MonoExtC_3 | 16 | 21 | PF00514 | 0.558 |
TRG_NLS_MonoExtC_3 | 438 | 443 | PF00514 | 0.638 |
TRG_Pf-PMV_PEXEL_1 | 117 | 121 | PF00026 | 0.419 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.347 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKR9 | Leptomonas seymouri | 83% | 100% |
A0A0S4JQF8 | Bodo saltans | 55% | 100% |
A0A1X0P5K5 | Trypanosomatidae | 67% | 100% |
A0A3R7M7F0 | Trypanosoma rangeli | 66% | 100% |
A0A3R7M8S7 | Trypanosoma rangeli | 24% | 91% |
A4IC39 | Leishmania infantum | 99% | 100% |
C9ZYD4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 100% |
E3TDS3 | Ictalurus punctatus | 26% | 100% |
E9AFZ4 | Leishmania major | 96% | 100% |
E9B747 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
O15827 | Leishmania braziliensis | 92% | 100% |
O74776 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
P53145 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 72% |
Q29AU5 | Drosophila pseudoobscura pseudoobscura | 28% | 100% |
Q4PS77 | Bos taurus | 28% | 100% |
Q8R2R6 | Mus musculus | 29% | 100% |
Q9BT17 | Homo sapiens | 29% | 100% |
Q9VCU5 | Drosophila melanogaster | 27% | 100% |
V5BTY1 | Trypanosoma cruzi | 65% | 100% |