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 |
Related structures:
AlphaFold database: A4HDM6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.373 |
CLV_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.578 |
CLV_C14_Caspase3-7 | 505 | 509 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.400 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.250 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.695 |
CLV_PCSK_PC1ET2_1 | 202 | 204 | PF00082 | 0.398 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.303 |
CLV_PCSK_PC1ET2_1 | 67 | 69 | PF00082 | 0.745 |
CLV_PCSK_PC7_1 | 10 | 16 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.388 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.600 |
DEG_SCF_FBW7_2 | 118 | 123 | PF00400 | 0.490 |
DEG_SPOP_SBC_1 | 174 | 178 | PF00917 | 0.301 |
DEG_SPOP_SBC_1 | 245 | 249 | PF00917 | 0.515 |
DEG_SPOP_SBC_1 | 57 | 61 | PF00917 | 0.647 |
DOC_CKS1_1 | 491 | 496 | PF01111 | 0.533 |
DOC_CYCLIN_RxL_1 | 200 | 209 | PF00134 | 0.347 |
DOC_CYCLIN_yCln2_LP_2 | 103 | 109 | PF00134 | 0.523 |
DOC_MAPK_gen_1 | 165 | 173 | PF00069 | 0.314 |
DOC_MAPK_MEF2A_6 | 277 | 286 | PF00069 | 0.269 |
DOC_MAPK_RevD_3 | 190 | 203 | PF00069 | 0.487 |
DOC_PP2B_LxvP_1 | 231 | 234 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 364 | 367 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.509 |
DOC_PP2B_LxvP_1 | 445 | 448 | PF13499 | 0.480 |
DOC_PP4_FxxP_1 | 218 | 221 | PF00568 | 0.337 |
DOC_SPAK_OSR1_1 | 380 | 384 | PF12202 | 0.488 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.762 |
DOC_USP7_UBL2_3 | 140 | 144 | PF12436 | 0.428 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.579 |
LIG_14-3-3_CanoR_1 | 159 | 165 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 324 | 331 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 88 | 97 | PF00244 | 0.664 |
LIG_Actin_WH2_2 | 283 | 301 | PF00022 | 0.538 |
LIG_Actin_WH2_2 | 96 | 112 | PF00022 | 0.349 |
LIG_BIR_III_2 | 250 | 254 | PF00653 | 0.493 |
LIG_eIF4E_1 | 306 | 312 | PF01652 | 0.538 |
LIG_EVH1_2 | 96 | 100 | PF00568 | 0.423 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.465 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.283 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.437 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.424 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.371 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.526 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.560 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.443 |
LIG_LIR_Apic_2 | 217 | 221 | PF02991 | 0.332 |
LIG_LIR_Apic_2 | 433 | 439 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 474 | 482 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 474 | 479 | PF02991 | 0.389 |
LIG_PDZ_Class_1 | 512 | 517 | PF00595 | 0.641 |
LIG_Pex14_1 | 436 | 440 | PF04695 | 0.478 |
LIG_SH2_CRK | 306 | 310 | PF00017 | 0.460 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.380 |
LIG_SH3_1 | 10 | 16 | PF00018 | 0.620 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.688 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.321 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.549 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.460 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.490 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.718 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.564 |
LIG_SUMO_SIM_anti_2 | 307 | 313 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 105 | 111 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 418 | 425 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 477 | 483 | PF11976 | 0.531 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.591 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.538 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.538 |
LIG_TYR_ITIM | 438 | 443 | PF00017 | 0.503 |
LIG_WRC_WIRS_1 | 452 | 457 | PF05994 | 0.461 |
MOD_CDK_SPxxK_3 | 329 | 336 | PF00069 | 0.460 |
MOD_CDK_SPxxK_3 | 391 | 398 | PF00069 | 0.384 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.683 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.503 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.526 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.461 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.704 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.544 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.708 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.580 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.536 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.753 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.360 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.360 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.493 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.627 |
MOD_GlcNHglycan | 406 | 411 | PF01048 | 0.361 |
MOD_GlcNHglycan | 431 | 435 | PF01048 | 0.212 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.759 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.500 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.399 |
MOD_GlcNHglycan | 513 | 517 | PF01048 | 0.489 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.503 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.778 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.521 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.491 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.558 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.472 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.305 |
MOD_N-GLC_1 | 455 | 460 | PF02516 | 0.272 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.644 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.523 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.501 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.559 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.538 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.460 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.436 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.414 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.404 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.549 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.488 |
MOD_Plk_2-3 | 498 | 504 | PF00069 | 0.637 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.483 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.416 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.538 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.462 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.419 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.331 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.460 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.571 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.736 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.751 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.571 |
TRG_DiLeu_BaEn_1 | 227 | 232 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.702 |
TRG_Pf-PMV_PEXEL_1 | 427 | 431 | PF00026 | 0.236 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1U8 | Leptomonas seymouri | 63% | 100% |
A0A0S4JI78 | Bodo saltans | 43% | 100% |
A0A1X0NVU0 | Trypanosomatidae | 45% | 100% |
A0A3Q8IBF1 | Leishmania donovani | 79% | 100% |
A0A3R7R8W6 | Trypanosoma rangeli | 46% | 100% |
C9ZWD9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AH73 | Leishmania infantum | 79% | 100% |
E9AX11 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QAG5 | Leishmania major | 81% | 100% |
V5BFK4 | Trypanosoma cruzi | 48% | 100% |