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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 4 |
Related structures:
AlphaFold database: A4HI91
Term | Name | Level | Count |
---|---|---|---|
GO:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 144 | 148 | PF00656 | 0.550 |
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.490 |
CLV_C14_Caspase3-7 | 416 | 420 | PF00656 | 0.368 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.590 |
CLV_PCSK_FUR_1 | 69 | 73 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 387 | 389 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.386 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.497 |
DEG_SCF_FBW7_1 | 443 | 449 | PF00400 | 0.247 |
DOC_CKS1_1 | 443 | 448 | PF01111 | 0.309 |
DOC_CKS1_1 | 82 | 87 | PF01111 | 0.494 |
DOC_CYCLIN_yCln2_LP_2 | 195 | 198 | PF00134 | 0.303 |
DOC_MAPK_gen_1 | 471 | 479 | PF00069 | 0.248 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.303 |
DOC_PP4_FxxP_1 | 531 | 534 | PF00568 | 0.373 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.383 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.316 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 264 | 272 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 421 | 430 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 471 | 480 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.787 |
LIG_14-3-3_CanoR_1 | 521 | 530 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.802 |
LIG_APCC_ABBA_1 | 405 | 410 | PF00400 | 0.426 |
LIG_BIR_III_4 | 419 | 423 | PF00653 | 0.417 |
LIG_BRCT_BRCA1_1 | 210 | 214 | PF00533 | 0.454 |
LIG_Clathr_ClatBox_1 | 189 | 193 | PF01394 | 0.311 |
LIG_deltaCOP1_diTrp_1 | 258 | 265 | PF00928 | 0.432 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.282 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.473 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.459 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.432 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.511 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.496 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.271 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.508 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.389 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.643 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.622 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.596 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.404 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.327 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.283 |
LIG_Integrin_isoDGR_2 | 503 | 505 | PF01839 | 0.447 |
LIG_LIR_Apic_2 | 168 | 174 | PF02991 | 0.498 |
LIG_LIR_Apic_2 | 529 | 534 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 352 | 362 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 352 | 357 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.497 |
LIG_PCNA_yPIPBox_3 | 411 | 421 | PF02747 | 0.262 |
LIG_SH2_STAP1 | 323 | 327 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 488 | 492 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 518 | 522 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.418 |
LIG_SH3_2 | 25 | 30 | PF14604 | 0.507 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.674 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.239 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.410 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.526 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.387 |
LIG_SH3_4 | 427 | 434 | PF00018 | 0.408 |
LIG_SUMO_SIM_par_1 | 413 | 419 | PF11976 | 0.244 |
LIG_SUMO_SIM_par_1 | 452 | 458 | PF11976 | 0.381 |
LIG_WRC_WIRS_1 | 439 | 444 | PF05994 | 0.447 |
MOD_CDK_SPxxK_3 | 145 | 152 | PF00069 | 0.647 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.621 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.664 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.480 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.560 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.466 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.786 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.506 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.519 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.380 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.445 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.718 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.634 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.473 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.268 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.278 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.268 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.368 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.153 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.498 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.597 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.402 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.353 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.581 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.601 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.708 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.473 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.378 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.686 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.318 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.479 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.543 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.233 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.316 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.716 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.700 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.489 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.320 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.586 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.500 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.379 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.273 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.436 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.424 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.324 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.484 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.647 |
MOD_NEK2_2 | 323 | 328 | PF00069 | 0.432 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.638 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.461 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.513 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.550 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.769 |
MOD_PK_1 | 30 | 36 | PF00069 | 0.621 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.747 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.711 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.790 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.549 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.473 |
MOD_Plk_2-3 | 239 | 245 | PF00069 | 0.368 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.510 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.313 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.447 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.372 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.665 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.489 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.320 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.350 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.568 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.690 |
MOD_SUMO_rev_2 | 239 | 249 | PF00179 | 0.379 |
MOD_SUMO_rev_2 | 273 | 280 | PF00179 | 0.432 |
MOD_SUMO_rev_2 | 542 | 546 | PF00179 | 0.274 |
TRG_DiLeu_BaEn_1 | 512 | 517 | PF01217 | 0.381 |
TRG_DiLeu_BaLyEn_6 | 451 | 456 | PF01217 | 0.357 |
TRG_DiLeu_BaLyEn_6 | 502 | 507 | PF01217 | 0.414 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 264 | 268 | PF00026 | 0.326 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHN2 | Leptomonas seymouri | 21% | 100% |
A0A0N1IMQ0 | Leptomonas seymouri | 68% | 100% |
A0A1X0P1V8 | Trypanosomatidae | 55% | 100% |
A0A3Q8IGC4 | Leishmania donovani | 24% | 100% |
A0A3Q8IHW0 | Leishmania donovani | 80% | 100% |
A0A3R7MF36 | Trypanosoma rangeli | 49% | 100% |
A0A3S7WR72 | Leishmania donovani | 23% | 100% |
A4H666 | Leishmania braziliensis | 23% | 100% |
A4HUJ0 | Leishmania infantum | 23% | 100% |
A4I135 | Leishmania infantum | 24% | 100% |
A4I5H1 | Leishmania infantum | 80% | 100% |
C9ZQV5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AN88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9AX72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B0R9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
P25382 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
Q4Q7G4 | Leishmania major | 79% | 100% |
Q4QAA4 | Leishmania major | 24% | 100% |
Q4QHD6 | Leishmania major | 23% | 100% |
V5BYY0 | Trypanosoma cruzi | 50% | 100% |