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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ASM5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004518 | nuclease activity | 4 | 11 |
GO:0004519 | endonuclease activity | 5 | 11 |
GO:0004521 | RNA endonuclease activity | 5 | 11 |
GO:0004525 | ribonuclease III activity | 6 | 11 |
GO:0004540 | RNA nuclease activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 11 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 11 |
GO:0032296 | double-stranded RNA-specific ribonuclease activity | 5 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.408 |
CLV_C14_Caspase3-7 | 428 | 432 | PF00656 | 0.475 |
CLV_MEL_PAP_1 | 554 | 560 | PF00089 | 0.572 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.761 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.771 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.720 |
CLV_PCSK_FUR_1 | 219 | 223 | PF00082 | 0.417 |
CLV_PCSK_FUR_1 | 79 | 83 | PF00082 | 0.782 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.760 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.767 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.720 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.379 |
CLV_Separin_Metazoa | 179 | 183 | PF03568 | 0.396 |
DEG_APCC_DBOX_1 | 220 | 228 | PF00400 | 0.511 |
DEG_APCC_DBOX_1 | 496 | 504 | PF00400 | 0.688 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.449 |
DEG_SCF_FBW7_1 | 447 | 453 | PF00400 | 0.586 |
DOC_ANK_TNKS_1 | 482 | 489 | PF00023 | 0.685 |
DOC_CDC14_PxL_1 | 205 | 213 | PF14671 | 0.422 |
DOC_CKS1_1 | 447 | 452 | PF01111 | 0.514 |
DOC_CKS1_1 | 59 | 64 | PF01111 | 0.723 |
DOC_CKS1_1 | 96 | 101 | PF01111 | 0.723 |
DOC_CYCLIN_yClb1_LxF_4 | 397 | 403 | PF00134 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 5 | 11 | PF00134 | 0.550 |
DOC_MAPK_DCC_7 | 2 | 12 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 219 | 229 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 26 | 34 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 393 | 402 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 78 | 86 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 123 | 132 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 173 | 180 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 26 | 34 | PF00069 | 0.568 |
DOC_MAPK_MEF2A_6 | 511 | 520 | PF00069 | 0.639 |
DOC_MAPK_MEF2A_6 | 557 | 565 | PF00069 | 0.503 |
DOC_MAPK_NFAT4_5 | 173 | 181 | PF00069 | 0.380 |
DOC_PP1_RVXF_1 | 256 | 262 | PF00149 | 0.394 |
DOC_PP2B_LxvP_1 | 5 | 8 | PF13499 | 0.651 |
DOC_PP2B_LxvP_1 | 565 | 568 | PF13499 | 0.603 |
DOC_PP2B_LxvP_1 | 93 | 96 | PF13499 | 0.753 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.724 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.301 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.572 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.283 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.703 |
LIG_14-3-3_CanoR_1 | 198 | 205 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 26 | 31 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 532 | 538 | PF00244 | 0.428 |
LIG_APCC_ABBA_1 | 140 | 145 | PF00400 | 0.388 |
LIG_BRCT_BRCA1_1 | 252 | 256 | PF00533 | 0.435 |
LIG_BRCT_BRCA1_1 | 275 | 279 | PF00533 | 0.526 |
LIG_DLG_GKlike_1 | 416 | 424 | PF00625 | 0.691 |
LIG_eIF4E_1 | 362 | 368 | PF01652 | 0.547 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.644 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.590 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.373 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.586 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.571 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.694 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.647 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.422 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.525 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.727 |
LIG_FXI_DFP_1 | 143 | 147 | PF00024 | 0.406 |
LIG_GBD_Chelix_1 | 329 | 337 | PF00786 | 0.348 |
LIG_Integrin_RGD_1 | 426 | 428 | PF01839 | 0.690 |
LIG_Integrin_RGDW_4 | 426 | 429 | PF00362 | 0.692 |
LIG_LIR_Apic_2 | 433 | 439 | PF02991 | 0.686 |
LIG_LIR_Apic_2 | 441 | 445 | PF02991 | 0.602 |
LIG_LIR_Gen_1 | 114 | 122 | PF02991 | 0.673 |
LIG_LIR_Gen_1 | 141 | 148 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 193 | 204 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 253 | 262 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 291 | 297 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 331 | 341 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 475 | 486 | PF02991 | 0.694 |
LIG_LIR_Gen_1 | 527 | 536 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 114 | 118 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 527 | 531 | PF02991 | 0.449 |
LIG_NRBOX | 222 | 228 | PF00104 | 0.390 |
LIG_PCNA_yPIPBox_3 | 385 | 395 | PF02747 | 0.524 |
LIG_PDZ_Class_3 | 575 | 580 | PF00595 | 0.561 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.658 |
LIG_Pex14_2 | 139 | 143 | PF04695 | 0.385 |
LIG_PTB_Apo_2 | 152 | 159 | PF02174 | 0.402 |
LIG_SH2_CRK | 436 | 440 | PF00017 | 0.742 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.734 |
LIG_SH2_GRB2like | 478 | 481 | PF00017 | 0.606 |
LIG_SH2_GRB2like | 56 | 59 | PF00017 | 0.704 |
LIG_SH2_STAP1 | 362 | 366 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 373 | 377 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.515 |
LIG_SH3_1 | 442 | 448 | PF00018 | 0.680 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.742 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.558 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.638 |
LIG_SUMO_SIM_anti_2 | 498 | 504 | PF11976 | 0.691 |
LIG_SUMO_SIM_anti_2 | 61 | 68 | PF11976 | 0.653 |
LIG_SUMO_SIM_par_1 | 128 | 135 | PF11976 | 0.589 |
LIG_UBA3_1 | 223 | 231 | PF00899 | 0.394 |
MOD_CDC14_SPxK_1 | 135 | 138 | PF00782 | 0.295 |
MOD_CDK_SPK_2 | 132 | 137 | PF00069 | 0.283 |
MOD_CDK_SPK_2 | 435 | 440 | PF00069 | 0.474 |
MOD_CDK_SPK_2 | 552 | 557 | PF00069 | 0.747 |
MOD_CDK_SPxK_1 | 132 | 138 | PF00069 | 0.286 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.727 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.494 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.656 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.534 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.694 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.710 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.495 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.475 |
MOD_Cter_Amidation | 49 | 52 | PF01082 | 0.744 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.698 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.549 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.712 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.515 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.631 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.692 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.701 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.693 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.509 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.725 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.569 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.450 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.667 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.722 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.592 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.644 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.657 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.413 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.583 |
MOD_N-GLC_1 | 524 | 529 | PF02516 | 0.500 |
MOD_N-GLC_2 | 200 | 202 | PF02516 | 0.550 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.561 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.430 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.485 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.541 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.371 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.630 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.706 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.678 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.654 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.708 |
MOD_NEK2_2 | 288 | 293 | PF00069 | 0.567 |
MOD_NEK2_2 | 514 | 519 | PF00069 | 0.641 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.548 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.659 |
MOD_PK_1 | 26 | 32 | PF00069 | 0.568 |
MOD_PK_1 | 557 | 563 | PF00069 | 0.453 |
MOD_PK_1 | 82 | 88 | PF00069 | 0.475 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.685 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.424 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.416 |
MOD_Plk_1 | 498 | 504 | PF00069 | 0.732 |
MOD_Plk_1 | 524 | 530 | PF00069 | 0.505 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.475 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.393 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.423 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.330 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.659 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.707 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.614 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.649 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.286 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.430 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.769 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.493 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.636 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.652 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.701 |
MOD_SUMO_for_1 | 570 | 573 | PF00179 | 0.673 |
TRG_AP2beta_CARGO_1 | 141 | 150 | PF09066 | 0.409 |
TRG_DiLeu_BaEn_1 | 88 | 93 | PF01217 | 0.688 |
TRG_DiLeu_BaEn_2 | 256 | 262 | PF01217 | 0.516 |
TRG_DiLeu_BaLyEn_6 | 219 | 224 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.704 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.763 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 520 | 522 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.710 |
TRG_NLS_Bipartite_1 | 137 | 153 | PF00514 | 0.402 |
TRG_NLS_MonoExtN_4 | 219 | 224 | PF00514 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 365 | 369 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3V7 | Leptomonas seymouri | 48% | 98% |
A0A1X0P9H0 | Trypanosomatidae | 49% | 100% |
A0A3R7KSN8 | Trypanosoma rangeli | 46% | 100% |
A0A3S7XAI5 | Leishmania donovani | 90% | 99% |
A4HNW5 | Leishmania braziliensis | 79% | 100% |
A4ICM9 | Leishmania infantum | 90% | 99% |
D0A2T3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
Q6T449 | Leishmania major | 88% | 100% |
V5BZU7 | Trypanosoma cruzi | 48% | 100% |