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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H9K5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.553 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.596 |
CLV_PCSK_FUR_1 | 437 | 441 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.761 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 430 | 432 | PF00082 | 0.652 |
CLV_PCSK_PC7_1 | 181 | 187 | PF00082 | 0.782 |
CLV_PCSK_PC7_1 | 433 | 439 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.481 |
CLV_Separin_Metazoa | 280 | 284 | PF03568 | 0.384 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.520 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.522 |
DOC_CKS1_1 | 75 | 80 | PF01111 | 0.525 |
DOC_MAPK_RevD_3 | 340 | 355 | PF00069 | 0.356 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.646 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.575 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.531 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 117 | 121 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 122 | 127 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 186 | 190 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 262 | 271 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 355 | 359 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 398 | 403 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 431 | 436 | PF00244 | 0.612 |
LIG_BRCT_BRCA1_1 | 241 | 245 | PF00533 | 0.797 |
LIG_CSL_BTD_1 | 257 | 260 | PF09270 | 0.540 |
LIG_CtBP_PxDLS_1 | 54 | 58 | PF00389 | 0.523 |
LIG_EVH1_2 | 93 | 97 | PF00568 | 0.499 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.687 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.582 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.719 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.540 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.606 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.527 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.556 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.541 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.470 |
LIG_MAD2 | 333 | 341 | PF02301 | 0.324 |
LIG_MYND_1 | 20 | 24 | PF01753 | 0.526 |
LIG_MYND_1 | 227 | 231 | PF01753 | 0.536 |
LIG_NRBOX | 189 | 195 | PF00104 | 0.481 |
LIG_PDZ_Class_3 | 467 | 472 | PF00595 | 0.670 |
LIG_Pex14_1 | 459 | 463 | PF04695 | 0.497 |
LIG_SH2_NCK_1 | 414 | 418 | PF00017 | 0.689 |
LIG_SH2_SRC | 463 | 466 | PF00017 | 0.470 |
LIG_SH2_STAT3 | 141 | 144 | PF00017 | 0.534 |
LIG_SH2_STAT3 | 65 | 68 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.693 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.510 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.523 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.781 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.733 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.508 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.511 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.511 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.496 |
LIG_TRAF2_1 | 327 | 330 | PF00917 | 0.576 |
LIG_WW_1 | 95 | 98 | PF00397 | 0.510 |
MOD_CDK_SPK_2 | 451 | 456 | PF00069 | 0.621 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.507 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.534 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.747 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.549 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.793 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.566 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.546 |
MOD_Cter_Amidation | 352 | 355 | PF01082 | 0.414 |
MOD_Cter_Amidation | 428 | 431 | PF01082 | 0.623 |
MOD_Cter_Amidation | 435 | 438 | PF01082 | 0.493 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.650 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.716 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.597 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.535 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.593 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.638 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.514 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.497 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.701 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.662 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.523 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.764 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.469 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.600 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.578 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.595 |
MOD_N-GLC_2 | 104 | 106 | PF02516 | 0.509 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.712 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.705 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.635 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.708 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.461 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.503 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.651 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.825 |
MOD_PIKK_1 | 324 | 330 | PF00454 | 0.667 |
MOD_PK_1 | 122 | 128 | PF00069 | 0.500 |
MOD_PK_1 | 431 | 437 | PF00069 | 0.609 |
MOD_PKA_1 | 185 | 191 | PF00069 | 0.747 |
MOD_PKA_1 | 354 | 360 | PF00069 | 0.432 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.701 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.777 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.688 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.656 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.370 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.408 |
MOD_Plk_2-3 | 200 | 206 | PF00069 | 0.667 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.734 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.824 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.599 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.668 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.512 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.656 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.567 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.577 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.535 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.516 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.525 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.530 |
MOD_SUMO_for_1 | 373 | 376 | PF00179 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 18 | 23 | PF01217 | 0.521 |
TRG_ER_diArg_1 | 437 | 440 | PF00400 | 0.650 |
TRG_NLS_MonoExtN_4 | 428 | 434 | PF00514 | 0.638 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I846 | Leptomonas seymouri | 53% | 100% |
A0A3Q8ID30 | Leishmania donovani | 75% | 100% |
A4HXW8 | Leishmania infantum | 76% | 100% |
E9ARN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QDU7 | Leishmania major | 77% | 100% |