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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:0032259 | methylation | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003723 | RNA binding | 4 | 9 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 9 |
GO:0008168 | methyltransferase activity | 4 | 10 |
GO:0008173 | RNA methyltransferase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.424 |
CLV_PCSK_FUR_1 | 523 | 527 | PF00082 | 0.418 |
CLV_PCSK_FUR_1 | 554 | 558 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 417 | 419 | PF00082 | 0.421 |
CLV_PCSK_PC7_1 | 418 | 424 | PF00082 | 0.420 |
CLV_PCSK_PC7_1 | 426 | 432 | PF00082 | 0.430 |
CLV_PCSK_PC7_1 | 525 | 531 | PF00082 | 0.526 |
CLV_PCSK_PC7_1 | 547 | 553 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.717 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.511 |
DEG_APCC_DBOX_1 | 304 | 312 | PF00400 | 0.369 |
DEG_APCC_DBOX_1 | 417 | 425 | PF00400 | 0.597 |
DEG_APCC_DBOX_1 | 433 | 441 | PF00400 | 0.412 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.770 |
DEG_ODPH_VHL_1 | 57 | 69 | PF01847 | 0.470 |
DEG_SPOP_SBC_1 | 368 | 372 | PF00917 | 0.528 |
DEG_SPOP_SBC_1 | 80 | 84 | PF00917 | 0.644 |
DOC_CKS1_1 | 209 | 214 | PF01111 | 0.518 |
DOC_CYCLIN_RxL_1 | 222 | 235 | PF00134 | 0.398 |
DOC_MAPK_gen_1 | 136 | 145 | PF00069 | 0.360 |
DOC_MAPK_gen_1 | 180 | 188 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 19 | 26 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 426 | 437 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 554 | 564 | PF00069 | 0.469 |
DOC_MAPK_JIP1_4 | 161 | 167 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 486 | 494 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 556 | 564 | PF00069 | 0.361 |
DOC_PP2B_LxvP_1 | 357 | 360 | PF13499 | 0.593 |
DOC_PP4_FxxP_1 | 207 | 210 | PF00568 | 0.377 |
DOC_PP4_FxxP_1 | 411 | 414 | PF00568 | 0.479 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.561 |
DOC_USP7_MATH_2 | 443 | 449 | PF00917 | 0.562 |
DOC_USP7_UBL2_3 | 96 | 100 | PF12436 | 0.378 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.557 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 190 | 198 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 28 | 35 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.766 |
LIG_14-3-3_CanoR_1 | 346 | 350 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 430 | 437 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 47 | 57 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 496 | 506 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 584 | 588 | PF00244 | 0.614 |
LIG_CSL_BTD_1 | 560 | 563 | PF09270 | 0.678 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.433 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.638 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.392 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.520 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.541 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.398 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.533 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.518 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.623 |
LIG_IRF3_LxIS_1 | 447 | 453 | PF10401 | 0.451 |
LIG_LIR_Apic_2 | 206 | 210 | PF02991 | 0.373 |
LIG_LIR_Apic_2 | 51 | 56 | PF02991 | 0.638 |
LIG_LIR_Apic_2 | 599 | 605 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 406 | 414 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 468 | 472 | PF02991 | 0.493 |
LIG_NRBOX | 239 | 245 | PF00104 | 0.446 |
LIG_NRP_CendR_1 | 604 | 607 | PF00754 | 0.585 |
LIG_PCNA_yPIPBox_3 | 543 | 557 | PF02747 | 0.550 |
LIG_RPA_C_Fungi | 540 | 552 | PF08784 | 0.446 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.282 |
LIG_SH2_CRK | 296 | 300 | PF00017 | 0.360 |
LIG_SH2_CRK | 602 | 606 | PF00017 | 0.685 |
LIG_SH2_SRC | 4 | 7 | PF00017 | 0.573 |
LIG_SH2_SRC | 469 | 472 | PF00017 | 0.573 |
LIG_SH2_STAP1 | 252 | 256 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 535 | 539 | PF00017 | 0.417 |
LIG_SH2_STAT3 | 313 | 316 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.418 |
LIG_SH3_1 | 53 | 59 | PF00018 | 0.524 |
LIG_SH3_1 | 557 | 563 | PF00018 | 0.485 |
LIG_SH3_2 | 210 | 215 | PF14604 | 0.409 |
LIG_SH3_2 | 560 | 565 | PF14604 | 0.515 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.478 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.254 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.674 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.529 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.606 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.519 |
LIG_SH3_CIN85_PxpxPR_1 | 356 | 361 | PF14604 | 0.644 |
LIG_SUMO_SIM_anti_2 | 183 | 189 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 227 | 232 | PF11976 | 0.320 |
LIG_TRAF2_1 | 381 | 384 | PF00917 | 0.580 |
LIG_TRAF2_1 | 474 | 477 | PF00917 | 0.503 |
LIG_TRFH_1 | 459 | 463 | PF08558 | 0.420 |
MOD_CDK_SPxxK_3 | 208 | 215 | PF00069 | 0.463 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.501 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.417 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.506 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.620 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.422 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.399 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.594 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.618 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.553 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.586 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.625 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.411 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.342 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.535 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.701 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.491 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.426 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.607 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.652 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.590 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.570 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.282 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.585 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.674 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.657 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.638 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.517 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.562 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.607 |
MOD_LATS_1 | 17 | 23 | PF00433 | 0.488 |
MOD_LATS_1 | 178 | 184 | PF00433 | 0.403 |
MOD_LATS_1 | 594 | 600 | PF00433 | 0.560 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.513 |
MOD_N-GLC_2 | 259 | 261 | PF02516 | 0.282 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.315 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.316 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.321 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.647 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.719 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.562 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.541 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.564 |
MOD_NEK2_2 | 283 | 288 | PF00069 | 0.390 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.723 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.591 |
MOD_PK_1 | 486 | 492 | PF00069 | 0.477 |
MOD_PKA_1 | 180 | 186 | PF00069 | 0.484 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.655 |
MOD_PKA_1 | 426 | 432 | PF00069 | 0.449 |
MOD_PKA_1 | 530 | 536 | PF00069 | 0.488 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.596 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.545 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.587 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.494 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.437 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.635 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.556 |
MOD_PKA_2 | 530 | 536 | PF00069 | 0.563 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.617 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.646 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.408 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.532 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.607 |
MOD_Plk_1 | 476 | 482 | PF00069 | 0.595 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.515 |
MOD_Plk_2-3 | 477 | 483 | PF00069 | 0.548 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.379 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.555 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.282 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.620 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.448 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.433 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.561 |
MOD_SUMO_for_1 | 287 | 290 | PF00179 | 0.413 |
TRG_DiLeu_BaEn_1 | 304 | 309 | PF01217 | 0.468 |
TRG_DiLeu_BaEn_2 | 516 | 522 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 431 | 436 | PF01217 | 0.499 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.491 |
TRG_ER_diArg_1 | 18 | 20 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 360 | 362 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 461 | 464 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 496 | 499 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 524 | 526 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 529 | 531 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 544 | 547 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 550 | 552 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 554 | 557 | PF00400 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 163 | 168 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 227 | 232 | PF00026 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 434 | 438 | PF00026 | 0.520 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEE8 | Leptomonas seymouri | 72% | 99% |
A0A1X0P5S3 | Trypanosomatidae | 50% | 100% |
A0A3S7X9F7 | Leishmania donovani | 93% | 100% |
A0A422P2S4 | Trypanosoma rangeli | 51% | 100% |
A4HMV6 | Leishmania braziliensis | 80% | 100% |
A4IBH7 | Leishmania infantum | 93% | 100% |
C9ZZ65 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AFB3 | Leishmania major | 92% | 100% |